Canonical Allele Identifier: PA2826228100
Gene: CCDC169-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_001185839.1:p.Val337Ile
CA6948859
NM_001198910.2:c.1009G>A