Canonical Allele Identifier: PA2829808820
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 283235
ClinVar RCV Id: RCV000298630 RCV000725237 RCV001079658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Val3827Leu
CA7221782
NM_015180.5:c.11479G>C
CA389942984
NM_015180.5:c.11479G>T