Canonical Allele Identifier: PA2828705117
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1359070
ClinVar RCV Id: RCV001894389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364202.1:p.Thr701Asn
CA6481487
NM_001377273.1:c.2102C>A