Canonical Allele Identifier: PA2573062258
Gene: ROM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 195063

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000318.2:p.Met271Thr
CA201529
NM_000327.4:c.812T>C