Canonical Allele Identifier: PA2827676717
Gene: ARMC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 427935
ClinVar RCV Id: RCV000491687 RCV000515496 RCV001034540 RCV001257948 RCV002527047
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339687.2:p.Gly459Arg
CA2160329
NM_001352758.2:c.1375G>A
CA350955987
NM_001352758.2:c.1375G>C