Canonical Allele Identifier: PA2827962387
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2562Cys
CA16037960
NM_001354897.2:c.7684A>T