Canonical Allele Identifier: PA2828012386
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gly2342Ser
CA013731
NM_001354905.2:c.7024G>A