Canonical Allele Identifier: PA2825092685
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1736284
ClinVar RCV Id: RCV002357563
ClinVar Variation Id: 2819276
ClinVar RCV Id: RCV003760967

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu1311Asp
CA072317
NM_000179.3:c.3933A>C
CA346761486
NM_000179.3:c.3933A>T