Allele Registry

Canonical Allele Identifier: PA2826634247

Gene: MSH6 HGNC NCBI

ClinVar Allele:

358721

ClinVar RCV:

RCV000410264

RCV000576046

RCV001361344

ClinVar Variation:

371790

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ser12Asn	CA073598 NM_001281494.2:c.35G>A