Canonical Allele Identifier: PA2828705801
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 520507

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364203.1:p.Arg332Gln
CA6481571
NM_001377274.1:c.995G>A