Canonical Allele Identifier: PA645486294
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 283946
ClinVar RCV Id: RCV000391945 RCV001112208
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Met303Val
CA7219272
NM_182914.2:c.907A>G