Canonical Allele Identifier: PA2825610646
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376691
ClinVar RCV Id: RCV000418604 RCV000418790 RCV000419222 RCV000421640 RCV000428839 RCV000426894 RCV000427499 RCV000428164 RCV000431867 RCV000436907 RCV000438411 RCV000437128 RCV000439967 RCV000441352 RCV000492782 RCV000530551 RCV000785304 RCV002289544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Tyr102His
CA16603104
NM_001126115.1:c.304T>C