Canonical Allele Identifier: PA2828053160
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser375Phe
CA005357
NM_001354905.2:c.1124C>T