Canonical Allele Identifier: PA2829467542
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 452908
ClinVar RCV Id: RCV000765698 RCV000727399 RCV001485096 RCV001563734 RCV001563735 RCV001272834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Pro1214Leu
CA1706667
NM_003494.4:c.3641C>T