Canonical Allele Identifier: PA2828705392
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 969387
ClinVar RCV Id: RCV001244724

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364202.1:p.Leu1093Val
CA384118142
NM_001377273.1:c.3277C>G