Canonical Allele Identifier: PA244658
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 196879
ClinVar RCV Id: RCV000177756 RCV001112395 RCV004020116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Phe1616Leu
CA244657
NM_182914.2:c.4846T>C
CA7220319
NM_182914.2:c.4848T>G
CA389937467
NM_182914.2:c.4848T>A