Canonical Allele Identifier: PA645436042
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376568
ClinVar RCV Id: RCV000417404 RCV000418478 RCV000423030 RCV000425219 RCV000427605 RCV000429427 RCV000433302 RCV000436176 RCV000435499 RCV000437866 RCV000444376 RCV000445236 RCV001214540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Cys9Phe
CA16602994
NM_001126117.1:c.26G>T