Allele Registry

Canonical Allele Identifier: PA2826633537

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001020925

RCV003314658

RCV003758984

ClinVar Variation:

824098

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Glu932Gln	CA46719355 NM_001281493.2:c.2794G>C