Canonical Allele Identifier: PA658679297
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_001119586.1:p.Met246Ile
CA287487993
NM_001126114.3:c.738G>A
CA397838990
NM_001126114.3:c.738G>T
CA397838992
NM_001126114.3:c.738G>C