Canonical Allele Identifier: PA2828705903
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 518779
ClinVar RCV Id: RCV000617611 RCV000624030 RCV001324563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364203.1:p.His442Gln
CA6481479
NM_001377274.1:c.1326C>A
CA384132355
NM_001377274.1:c.1326C>G