Canonical Allele Identifier: PA2829806632
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313484
ClinVar RCV Id: RCV001046788 RCV004021584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Asp118Val
CA7219088
NM_015180.5:c.353A>T