Canonical Allele Identifier: PA2573167512
Gene: ROM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1463622
ClinVar RCV Id: RCV001961145
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000318.2:p.Gly101Ser
CA6049694
NM_000327.4:c.301G>A