Canonical Allele Identifier: PA2829913661
Gene: THSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2305281
ClinVar RCV Id: RCV004151107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061146.1:p.Arg280Gly
CA388036718
NM_018676.4:c.838A>G