Canonical Allele Identifier: PA2580319004
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1741831

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Ala1535Asn
CA2580085257
NM_005691.3:c.4603_4604delinsAA