Canonical Allele Identifier: PA2829915776
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2129520
ClinVar RCV Id: RCV003050035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064693.2:p.Thr1053Pro
CA384118709
NM_020297.3:c.3157A>C