Canonical Allele Identifier: PA2828705396
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503002
ClinVar RCV Id: RCV002022614

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364202.1:p.Ala1098Glu
CA2573148552
NM_001377273.1:c.3293_3294delinsAA