Allele Registry

Canonical Allele Identifier: PA645385127

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000473620

RCV000571258

RCV002307506

RCV004001847

ClinVar Variation:

410496

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Asn1327Tyr	CA16611088 NM_000179.3:c.3979A>T