Canonical Allele Identifier: PA260098
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 35536
ClinVar RCV Id: RCV000029191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064693.2:p.His60Tyr
CA260095
NM_020297.3:c.178C>T