Canonical Allele Identifier: PA1139736917
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_064693.2:p.Cys515Ser
CA384139234
NM_020297.3:c.1544G>C
CA384139238
NM_020297.3:c.1543T>A