Canonical Allele Identifier: PA915973654
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 288008
ClinVar RCV Id: RCV000385438 RCV000525552 RCV001535516
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124454.1:p.Ala815Val
CA1706139
NM_001130982.2:c.2444C>T