Canonical Allele Identifier: PA110819
Gene: DYSF HGNC NCBI
ClinVar RCV:
RCV000007064
ClinVar Variation:
6677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Asp625Tyr
CA253909
NM_003494.4:c.1873G>T