Canonical Allele Identifier: PA2827999645
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2738Gly
CA015444
NM_001354901.2:c.8212A>G