Canonical Allele Identifier: PA2829467482
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 281301
ClinVar RCV Id: RCV000382528 RCV000648004 RCV001272831 RCV003243035
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Asp1163Asn
CA1706621
NM_003494.4:c.3487G>A