Canonical Allele Identifier: PA2826587757
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455322
ClinVar RCV Id: RCV000542178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu1058_Ter1059insLeuThrAspTyrIleGlySerPheGluLeuThrSerAspLysGlyGlyLysPheArgGlnHisTyrAspLeuIleAsnPheIlePhe
CA16617728
NM_001281494.2:c.3173_3175dup
CA46720482
NM_001281494.2:c.3176A>T