Canonical Allele Identifier: PA2825762159
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 499205
ClinVar RCV Id: RCV000593233 RCV001240944 RCV001834886
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124455.1:p.Pro218Leu
CA1705435
NM_001130983.2:c.653C>T