Canonical Allele Identifier: PA913200272
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp1532Ala
CA16031394
NM_001127510.3:c.4595A>C