Canonical Allele Identifier: PA2827939450
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ala15Val
CA16021438
NM_001354895.2:c.44C>T