Canonical Allele Identifier: PA2828007443
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr1537Ala
CA10578392
NM_001354905.2:c.4609A>G