Canonical Allele Identifier: PA915963905
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 648188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser445Arg
CA346744540
NM_000179.3:c.1333A>C
CA346744554
NM_000179.3:c.1335T>A
CA346744555
NM_000179.3:c.1335T>G