Canonical Allele Identifier: PA645472661
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 282765
ClinVar RCV Id: RCV000270967 RCV000325795 RCV000725139 RCV001084284 RCV001272823 RCV003920053
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Lys983Thr
CA1706371
NM_003494.4:c.2948A>C