Canonical Allele Identifier: PA2828705530
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 201621
ClinVar RCV Id: RCV000183238

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364202.1:p.Pro1299Leu
CA308206
NM_001377273.1:c.3896C>T