Canonical Allele Identifier: PA2828705722
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1005992
ClinVar RCV Id: RCV001302964 RCV002393719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364203.1:p.Ala179Val
CA6481665
NM_001377274.1:c.536C>T