Canonical Allele Identifier: PA645499818
Gene: PRPF31 HGNC NCBI

Linked Data

ClinVar Variation Id: 236422
ClinVar RCV Id: RCV000225613 RCV001854792
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056444.3:p.Leu41Val
CA309320833
NM_015629.4:c.121C>G