Canonical Allele Identifier: PA2828705072
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 240202
ClinVar RCV Id: RCV000227266 RCV002487076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364202.1:p.Thr659Ala
CA10583040
NM_001377273.1:c.1975A>G