ClinGen Allele Registry
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Canonical Allele Identifier:
PA105625
Gene: ABCC9
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000024625
RCV000256056
RCV000559460
RCV003335056
ClinVar Variation:
31947
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005682.2:p.Arg1154Gln
CA260062
NM_005691.3:c.3461G>A