Canonical Allele Identifier: PA2827993006
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser728Gly
CA031761
NM_001354901.2:c.2182A>G