Allele Registry

Canonical Allele Identifier: PA2826630772

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV004015602

ClinVar Variation:

3075076

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Glu302Ala	CA346749388 NM_001281493.2:c.905A>C