Canonical Allele Identifier: PA645392890
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 363294
ClinVar RCV Id: RCV000310533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Gln1290His
CA10627986
NM_006269.2:c.3870G>T
CA370997456
NM_006269.2:c.3870G>C