Allele Registry

Canonical Allele Identifier: PA330499

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000218375

RCV000409200

RCV000565213

RCV000627700

RCV000764427

RCV003460677

RCV003493433

ClinVar Variation:

89342

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ala1055Thr	CA011694 NM_000179.3:c.3163G>A