Canonical Allele Identifier: PA2573097089
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 448598
ClinVar RCV Id: RCV000517761 RCV000878962 RCV002060265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149062.2:p.Ala1165Val
CA4058838
NM_033071.5:c.3494C>T