Canonical Allele Identifier: PA2573074321
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 420903
ClinVar RCV Id: RCV000487267

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364203.1:p.Ser924Ala
CA16619502
NM_001377274.1:c.2770T>G