Canonical Allele Identifier: PA2825894589
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_001138987.1:p.Thr340Met
CA174292
NM_001145515.2:c.1019C>T