Canonical Allele Identifier: PA916004839
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 810744
ClinVar RCV Id: RCV000999582

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Ala1535Asp
CA6480805
NM_005691.3:c.4604C>A