Canonical Allele Identifier: PA645486478
Gene: SYNE2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Lys2921Gln
CA7221157
NM_182914.2:c.8761A>C