Canonical Allele Identifier: PA2828047684
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ala2346Val
CA013674
NM_001354904.2:c.7037C>T