Canonical Allele Identifier: PA2826673908
Gene: TCAIM HGNC NCBI

Linked Data

ClinVar Variation Id: 2552921
ClinVar RCV Id: RCV004326402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269842.1:p.His241Tyr
CA74466853
NM_001282913.2:c.721C>T