Allele Registry

Canonical Allele Identifier: PA110962

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000007069

RCV000594920

RCV003159090

ClinVar Variation:

6682

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Gly299Trp	CA253918 NM_003494.4:c.895G>T