Canonical Allele Identifier: PA2826632339
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 821928

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr664Ser
CA346756091
NM_001281493.2:c.1990A>T
CA346756094
NM_001281493.2:c.1991C>G