Canonical Allele Identifier: PA2828014437
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser12Gly
CA015623
NM_001354906.2:c.34A>G