Allele Registry

Canonical Allele Identifier: PA658806953

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000648011

RCV001563807

RCV001563808

RCV001563809

ClinVar Variation:

538640

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124459.1:p.Ile1623Val	CA1707160 NM_001130987.2:c.4867A>G