Canonical Allele Identifier: PA185939
Gene: TCF12 HGNC NCBI

Linked Data

ClinVar Variation Id: 127272
ClinVar RCV Id: RCV000157617
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996920.1:p.Arg613His
CA185937
NM_207037.2:c.1838G>A