Canonical Allele Identifier: PA174293
Gene: SCRN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 161537
ClinVar RCV Id: RCV000149072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138985.1:p.Thr408Met
CA174292
NM_001145513.1:c.1223C>T