Canonical Allele Identifier: PA2828012144
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ala2312Val
CA013674
NM_001354905.2:c.6935C>T