Canonical Allele Identifier: PA2829913647
Gene: THSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3177143
ClinVar RCV Id: RCV004466985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061146.1:p.Val166Ile
CA388038310
NM_018676.4:c.496G>A