Canonical Allele Identifier: PA207019
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 212345
ClinVar RCV Id: RCV000193493 RCV000556513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Lys174Arg
CA207018
NM_182914.2:c.521A>G