Canonical Allele Identifier: PA2828705751
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 45389
ClinVar RCV Id: RCV000038586 RCV000766938 RCV000792599 RCV002482998 RCV003162339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364203.1:p.Tyr247His
CA136215
NM_001377274.1:c.739T>C