Canonical Allele Identifier: PA2825093127
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455322
ClinVar RCV Id: RCV000542178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu1360_Ter1361insLeuThrAspTyrIleGlySerPheGluLeuThrSerAspLysGlyGlyLysPheArgGlnHisTyrAspLeuIleAsnPheIlePhe
CA16617728
NM_000179.3:c.4079_4081dup
CA46720482
NM_000179.3:c.4082A>T