Canonical Allele Identifier: PA2828705898
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1059229
ClinVar RCV Id: RCV001368467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364203.1:p.Thr436Ile
CA6481480
NM_001377274.1:c.1307C>T