Canonical Allele Identifier: PA2825609699
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376641
ClinVar RCV Id: RCV000418125 RCV000419693 RCV000420971 RCV000420838 RCV000425371 RCV000428371 RCV000426064 RCV000426471 RCV000431059 RCV000432886 RCV000431789 RCV000436762 RCV000437396 RCV000438632 RCV000441351 RCV000443299 RCV000443386 RCV000459465 RCV002338981
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Pro19Ala
CA16603058
NM_001126115.1:c.55C>G