Canonical Allele Identifier: PA645472085
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418425
ClinVar RCV Id: RCV000479816 RCV001075073 RCV001250369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Trp174Cys
CA16618286
NM_000322.5:c.522G>C
CA364137372
NM_000322.5:c.522G>T