Canonical Allele Identifier: PA2827974016
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg471Gly
CA005217
NM_001354899.2:c.1411C>G