Canonical Allele Identifier: PA645510128
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 437965
ClinVar RCV Id: RCV000787665 RCV000504827 RCV001051123 RCV001074827 RCV002248741 RCV001250285 RCV001530240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Gly208Asp
CA3808568
NM_000322.5:c.623G>A