Canonical Allele Identifier: PA2741931001
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2823040
ClinVar RCV Id: RCV003714367
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Leu1252Phe
CA370997202
NM_006269.2:c.3756G>C
CA370997203
NM_006269.2:c.3756G>T