Canonical Allele Identifier: PA916039540
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg517Gly
CA005217
NM_001354896.2:c.1549C>G