Canonical Allele Identifier: PA658806631
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 538621
ClinVar RCV Id: RCV000647984 RCV001253301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Asn103Ser
CA1705307
NM_001130987.2:c.308A>G