Canonical Allele Identifier: PA2827941117
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Val530Ala
CA028518
NM_001354895.2:c.1589T>C