Canonical Allele Identifier: PA2830089995
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 502729
ClinVar RCV Id: RCV000592211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149062.2:p.Met8719Ile
CA366088780
NM_033071.5:c.26157G>T
CA366088782
NM_033071.5:c.26157G>C
CA366088784
NM_033071.5:c.26157G>A