Canonical Allele Identifier: PA102329
Gene: RMND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 39765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060379.2:p.Arg417Gln
CA130537
NM_017909.4:c.1250G>A