Canonical Allele Identifier: PA2828008060
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn1638Asp
CA010373
NM_001354905.2:c.4912A>G