Canonical Allele Identifier: PA2580114333
Gene: ROM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1897593
ClinVar RCV Id: RCV002572470

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000318.2:p.Leu46Arg
CA6049652
NM_000327.4:c.137T>G