Canonical Allele Identifier: PA2830086062
Gene: SYNE1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149062.2:p.Leu4702Phe
CA366098096
NM_033071.5:c.14106A>C
CA366098098
NM_033071.5:c.14106A>T