Canonical Allele Identifier: PA2830422012
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313668

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878914.1:p.Pro368Ser
CA7224941
NM_182910.2:c.1102C>T