Canonical Allele Identifier: PA2741814732
Gene: ROM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3004734
ClinVar RCV Id: RCV003860837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000318.2:p.Ser87Ile
CA6049683
NM_000327.4:c.260G>T