Canonical Allele Identifier: PA2828013620
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 957959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Met2553Val
CA16039002
NM_001354905.2:c.7657A>G