Canonical Allele Identifier: PA1139675128
Gene: ROM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 942568
ClinVar RCV Id: RCV001212578 RCV003890360
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000318.2:p.Gly111Trp
CA6049708
NM_000327.4:c.331G>T