Canonical Allele Identifier: PA645392885
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 281509
ClinVar RCV Id: RCV000313881 RCV000962335 RCV001002272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Lys1044Asn
CA4751646
NM_006269.2:c.3132A>C
CA370995552
NM_006269.2:c.3132A>T