Canonical Allele Identifier: PA1139737048
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 963322
ClinVar RCV Id: RCV001237332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064693.2:p.Ile718Val
CA384132637
NM_020297.3:c.2152A>G