Canonical Allele Identifier: PA2826563187
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376682
ClinVar RCV Id: RCV000418952 RCV000419588 RCV000421235 RCV000421916 RCV000424047 RCV000428672 RCV000426974 RCV000429233 RCV000429897 RCV000431494 RCV000434394 RCV000436627 RCV000439588 RCV000438926 RCV000443993 RCV000443853
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Tyr46Phe
CA16603096
NM_001276698.3:c.137A>T