Canonical Allele Identifier: PA2827954198
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469801

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gly6Ser
CA124925107
NM_001354897.2:c.16G>A