Canonical Allele Identifier: PA645504894
Gene: TACSTD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 297766
ClinVar RCV Id: RCV000386862 RCV003546502 RCV004021444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002344.2:p.Gly276Asp
CA877323
NM_002353.3:c.827G>A