Canonical Allele Identifier: PA2829887780
Gene: SOHLH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3138772
ClinVar RCV Id: RCV004435132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060296.2:p.Val260Ile
CA6948859
NM_017826.3:c.778G>A