ClinGen Allele Registry
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Canonical Allele Identifier:
PA645472244
Gene: PRPH2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
356777
ClinVar RCV Id:
RCV000271221
RCV000267701
RCV000311099
RCV000326330
RCV000362139
RCV000365732
RCV001250375
RCV001318786
RCV001530369
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000313.2:p.Ser217Gly
CA3808563
NM_000322.5:c.649A>G