Canonical Allele Identifier: PA645477006
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 94322
ClinVar RCV Id: RCV000080288 RCV000274365 RCV000331836 RCV000647983 RCV001276718 RCV004019553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Pro144Gln
CA222166
NM_001130987.2:c.431C>A