Canonical Allele Identifier: PA2828706176
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 201621
ClinVar RCV Id: RCV000183238

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364203.1:p.Pro1010Leu
CA308206
NM_001377274.1:c.3029C>T