Canonical Allele Identifier: PA658806611
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 502553
ClinVar RCV Id: RCV000596018 RCV000814681 RCV001829688 RCV002532670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Asn44Lys
CA1705231
NM_001130987.2:c.132C>A
CA347216072
NM_001130987.2:c.132C>G