Canonical Allele Identifier: PA2573167517
Gene: ROM1 HGNC NCBI
ClinVar RCV:
RCV001876740
ClinVar Variation:
1356498
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000318.2:p.Ala109Thr
CA6049701
NM_000327.4:c.325G>A