Canonical Allele Identifier: PA2826806284
Gene: ARMC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 427932
ClinVar RCV Id: RCV000491717 RCV000515505 RCV001034537 RCV001257947 RCV001038181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278585.2:p.Arg343Cys
CA2160165
NM_001291656.2:c.1027C>T