Canonical Allele Identifier: PA2826601078
Gene: SOHLH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3037787
ClinVar RCV Id: RCV003907285
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269076.1:p.Thr35Ile
CA6949033
NM_001282147.2:c.104C>T