Canonical Allele Identifier: PA2741814719
Gene: ROM1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000318.2:p.Val4Met
CA380967878
NM_000327.4:c.10G>A