Allele Registry

Canonical Allele Identifier: PA2826625440

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000074633

RCV000162441

RCV000202023

RCV000518839

RCV000524101

RCV001201190

RCV003162468

RCV003450922

ClinVar Variation:

89172

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Leu240Ser	CA008059 NM_001281492.2:c.719T>C