Canonical Allele Identifier: PA2580336835
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2074906
ClinVar RCV Id: RCV002982342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Asp1377Glu
CA4751804
NM_006269.2:c.4131C>G
CA370981335
NM_006269.2:c.4131C>A