Canonical Allele Identifier: PA2828046226
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro2126Ala
CA012481
NM_001354904.2:c.6376C>G