Canonical Allele Identifier: PA2580128944
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 2194013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Pro107Ser
CA354496873
NM_000539.3:c.319C>T