Canonical Allele Identifier: PA2827146878
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_001309083.1:p.Arg394His
CA185937
NM_001322154.2:c.1181G>A