Canonical Allele Identifier: PA185938
Gene: TCF12 HGNC NCBI

Linked Data

ClinVar Variation Id: 127272
ClinVar RCV Id: RCV000157617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996919.1:p.Arg613His
CA185937
NM_207036.2:c.1838G>A