Canonical Allele Identifier: PA2827562982
Gene: KRIT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 450697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337611.1:p.Thr457Ala
CA368147183
NM_001350682.1:c.1369A>G