Canonical Allele Identifier: PA2826635656
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1784993
ClinVar RCV Id: RCV002420022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ala381Thr
CA346750753
NM_001281494.2:c.1141G>A