Canonical Allele Identifier: PA2573167490
Gene: ROM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1525966
ClinVar RCV Id: RCV002037084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000318.2:p.Thr51Ile
CA380968652
NM_000327.4:c.152C>T