Canonical Allele Identifier: PA2829809853
Gene: SYNE2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Gln5376Arg
CA7223284
NM_015180.5:c.16127A>G