Canonical Allele Identifier: PA645441520
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 410821
ClinVar RCV Id: RCV000474937 RCV002496784 RCV000756944 RCV004022837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064693.2:p.Val867Ile
CA6481332
NM_020297.3:c.2599G>A