Canonical Allele Identifier: PA2573247567
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1479100
ClinVar RCV Id: RCV001990865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Glu1521Asp
CA384129305
NM_005691.3:c.4563G>T
CA384129307
NM_005691.3:c.4563G>C