Canonical Allele Identifier: PA2826956591
Gene: THSD7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3177248
ClinVar RCV Id: RCV004467090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303278.1:p.Gly59Arg
CA1890254
NM_001316349.2:c.175G>A
CA348411118
NM_001316349.2:c.175G>C