Canonical Allele Identifier: PA2828015929
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr417Met
CA028394
NM_001354903.2:c.1250C>T