Canonical Allele Identifier: PA2828007299
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1707985

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Val1515Gly
CA16032325
NM_001354905.2:c.4544T>G