Canonical Allele Identifier: PA2827987051
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gly1680Asp
CA10578397
NM_001354900.2:c.5039G>A