Canonical Allele Identifier: PA098905
Gene: PRPF31 HGNC NCBI

Linked Data

ClinVar Variation Id: 4362
ClinVar RCV Id: RCV000004610
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056444.3:p.Ala194Glu
CA253137
NM_015629.4:c.581C>A