Canonical Allele Identifier: PA2573062246
Gene: ROM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 193085
ClinVar RCV Id: RCV000724496 RCV001103768 RCV003888610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000318.2:p.Arg16His
CA238591
NM_000327.4:c.47G>A