Canonical Allele Identifier: PA103971
Gene: SYT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 431484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129277.1:p.Ile368Thr
CA385931875
NM_001135805.2:c.1103T>C