Canonical Allele Identifier: PA645486506
Gene: SYNE2 HGNC NCBI
ClinVar RCV:
RCV000337037
ClinVar Variation:
313553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Lys3499Gln
CA7221535
NM_182914.2:c.10495A>C