Canonical Allele Identifier: PA2828705737
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 836079
ClinVar RCV Id: RCV001037115
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364203.1:p.Cys227Ser
CA384139234
NM_001377274.1:c.680G>C
CA384139238
NM_001377274.1:c.679T>A