Canonical Allele Identifier: PA2828012836
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 957959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Met2622Val
CA16039002
NM_001354902.2:c.7864A>G