Canonical Allele Identifier: PA2825024742
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 921617
ClinVar RCV Id: RCV001181165

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2572Leu
CA16038090
NM_000038.6:c.7715C>T