Allele Registry

Canonical Allele Identifier: PA2826631193

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000130187

RCV000480300

RCV000524131

RCV000662368

RCV003320553

RCV003466939

ClinVar Variation:

89251

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Gln396Glu	CA009674 NM_001281493.2:c.1186C>G