Canonical Allele Identifier: PA2829915797
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1001549
ClinVar RCV Id: RCV001297868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064693.2:p.Leu1089Gln
CA384118177
NM_020297.3:c.3266T>A