Canonical Allele Identifier: PA2828705037
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 520507

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364202.1:p.Arg620Gln
CA6481571
NM_001377273.1:c.1859G>A