Canonical Allele Identifier: PA2573098338
Gene: ROMO1 HGNC NCBI
ClinVar RCV:
RCV001753181
ClinVar Variation:
1318406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542786.1:p.Gly9Arg
CA9837401
NM_080748.3:c.25G>A
CA408772482
NM_080748.3:c.25G>C