Canonical Allele Identifier: PA645486477
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313537
ClinVar RCV Id: RCV000814351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Glu2897Asp
CA7221146
NM_182914.2:c.8691G>C
CA389970115
NM_182914.2:c.8691G>T