Canonical Allele Identifier: PA2827947440
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ala2472Val
CA013674
NM_001354895.2:c.7415C>T