Canonical Allele Identifier: PA2829610774
Gene: TCF20 HGNC NCBI

Linked Data

ClinVar Variation Id: 1213736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005641.1:p.Pro632Thr
CA411789851
NM_005650.4:c.1894C>A