Canonical Allele Identifier: PA179984
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 167016
ClinVar RCV Id: RCV000153173 RCV001140455
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Ala170Val
CA179983
NM_003494.4:c.509C>T