Canonical Allele Identifier: PA2825766951
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 538623
ClinVar RCV Id: RCV000647986 RCV000765696 RCV001662702 RCV001835043
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Tyr540His
CA1705873
NM_001130985.2:c.1618T>C