Canonical Allele Identifier: PA916055930
Gene: ARMC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 427930
ClinVar RCV Id: RCV000491981 RCV000515488 RCV001034532 RCV001362306
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079415.4:p.Gly69Arg
CA2159877
NM_025139.6:c.205G>A
CA350945883
NM_025139.6:c.205G>C