Canonical Allele Identifier: PA2828047654
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2342Ala
CA047997
NM_001354904.2:c.7024T>G