Canonical Allele Identifier: PA2826806344
Gene: ARMC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 427939
ClinVar RCV Id: RCV000490882 RCV000515503 RCV001034533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278585.2:p.Arg446Cys
CA2160301
NM_001291656.2:c.1336C>T