Canonical Allele Identifier: PA645442588
Gene: TGFBI HGNC NCBI

Linked Data

ClinVar Variation Id: 350886

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000349.1:p.His438Tyr
CA3420348
NM_000358.3:c.1312C>T