Canonical Allele Identifier: PA2829915781
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 973522
ClinVar RCV Id: RCV001250144

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064693.2:p.Ala1064Pro
CA384118511
NM_020297.3:c.3190G>C