Canonical Allele Identifier: PA2827992297
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser476Phe
CA005357
NM_001354901.2:c.1427C>T