Canonical Allele Identifier: PA104958
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13014
ClinVar RCV Id: RCV000013888 RCV000490027 RCV000504743 RCV001075874 RCV000626702 RCV003989284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Pro347Leu
CA256662
NM_000539.3:c.1040C>T