Canonical Allele Identifier: PA105606
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 35534
ClinVar RCV Id: RCV000029189 RCV001249678 RCV001699182 RCV000809546 RCV002321487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Arg1116Cys
CA260087
NM_005691.3:c.3346C>T