Canonical Allele Identifier: PA645392892
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 426263
ClinVar RCV Id: RCV000726741 RCV001074453 RCV002526011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Phe1344Leu
CA4751791
NM_006269.2:c.4030T>C
CA370981106
NM_006269.2:c.4032T>A
CA370981107
NM_006269.2:c.4032T>G