Canonical Allele Identifier: PA2825764145
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 471324
ClinVar RCV Id: RCV000533199 RCV001834801 RCV001755866
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124455.1:p.Arg2066Trp
CA1707654
NM_001130983.2:c.6196C>T