Canonical Allele Identifier: PA222167
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_003485.1:p.Pro143Gln
CA222166
NM_003494.4:c.428C>A