Canonical Allele Identifier: PA2827677043
Gene: ARMC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 427939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339688.2:p.Arg446Cys
CA2160301
NM_001352759.2:c.1336C>T