Canonical Allele Identifier: PA2827147358
Gene: TCF12 HGNC NCBI

Linked Data

ClinVar Variation Id: 127272
ClinVar RCV Id: RCV000157617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309086.1:p.Arg589His
CA185937
NM_001322157.3:c.1766G>A