Canonical Allele Identifier: PA104476
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13042
ClinVar RCV Id: RCV000013917 RCV000132598 RCV001203907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Asn15Ser
CA256685
NM_000539.3:c.44A>G