Canonical Allele Identifier: PA2826567305
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 480961
ClinVar RCV Id: RCV000561491 RCV000633390 RCV003483672
ClinVar Variation Id: 968639
ClinVar RCV Id: RCV001243824
ClinVar Variation Id: 1758655
ClinVar RCV Id: RCV002380451
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Met207Ile
CA287487993
NM_001276761.3:c.621G>A
CA397838990
NM_001276761.3:c.621G>T
CA397838992
NM_001276761.3:c.621G>C