Allele Registry

Canonical Allele Identifier: PA2826633347

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001804702

ClinVar Variation:

1332186

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Ser893Asn	CA346760521 NM_001281493.2:c.2678G>A