Canonical Allele Identifier: PA2573062247
Gene: ROM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 193087
ClinVar RCV Id: RCV000173112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000318.2:p.Trp22Gly
CA238595
NM_000327.4:c.64T>G