Canonical Allele Identifier: PA645471896
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 285861
ClinVar RCV Id: RCV000403427 RCV000791184 RCV001165007 RCV001165008 RCV001165009 RCV001165010 RCV001165012 RCV001165011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Arg123Trp
CA3808629
NM_000322.5:c.367C>T