Allele Registry

Canonical Allele Identifier: PA2825759756

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000648011

RCV001563807

RCV001563808

RCV001563809

ClinVar Variation:

538640

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124453.1:p.Ile1622Val	CA1707160 NM_001130981.2:c.4864A>G