Canonical Allele Identifier: PA2828012695
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2395Ala
CA16037981
NM_001354905.2:c.7183T>G