Canonical Allele Identifier: PA645504888
Gene: TACSTD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 297770
ClinVar RCV Id: RCV000279707 RCV002522134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002344.2:p.Glu147Asp
CA877427
NM_002353.3:c.441G>C
CA340525860
NM_002353.3:c.441G>T