Canonical Allele Identifier: PA2828055291
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Met854Val
CA16027984
NM_001354905.2:c.2560A>G