Canonical Allele Identifier: PA2499231164
Gene: ROM1 HGNC NCBI
ClinVar RCV:
RCV001347878
ClinVar Variation:
1043729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000318.2:p.Val34Ile
CA6049648
NM_000327.4:c.100G>A