Canonical Allele Identifier: PA2827676051
Gene: ARMC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 427935
ClinVar RCV Id: RCV000491687 RCV000515496 RCV001034540 RCV001257948 RCV002527047
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339685.2:p.Gly492Arg
CA2160329
NM_001352756.2:c.1474G>A
CA350955987
NM_001352756.2:c.1474G>C