Canonical Allele Identifier: PA2828014075
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2637Gly
CA015444
NM_001354905.2:c.7909A>G