Canonical Allele Identifier: PA2827675821
Gene: ARMC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 427930
ClinVar RCV Id: RCV000491981 RCV000515488 RCV001034532 RCV001362306
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339685.2:p.Gly69Arg
CA2159877
NM_001352756.2:c.205G>A
CA350945883
NM_001352756.2:c.205G>C