Allele Registry

Canonical Allele Identifier: PA2829807362

Gene: SYNE2 HGNC NCBI

ClinVar RCV:

RCV000177756

RCV001112395

RCV004020116

ClinVar Variation:

196879

HGVS (amino-acid)	Matching Registered Transcripts
NP_055995.4:p.Phe1616Leu	CA244657 NM_015180.5:c.4846T>C CA7220319 NM_015180.5:c.4848T>G CA389937467 NM_015180.5:c.4848T>A