Allele Registry

Canonical Allele Identifier: PA357564

Gene: MSH6 HGNC NCBI

ClinVar Allele:

221311

ClinVar RCV:

RCV000205455

RCV000217289

RCV000519500

RCV001711360

RCV003997660

ClinVar Variation:

220943

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Asn1327Ser	CA072431 NM_000179.3:c.3980A>G