Canonical Allele Identifier: PA2741964788
Gene: SOHLH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3037787
ClinVar RCV Id: RCV003907285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060296.2:p.Thr35Ile
CA6949033
NM_017826.3:c.104C>T