Canonical Allele Identifier: PA2829808277
Gene: SYNE2 HGNC NCBI
ClinVar RCV:
RCV001061448
ClinVar Variation:
313546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Lys3135Arg
CA7221263
NM_015180.5:c.9404A>G