Allele Registry

Canonical Allele Identifier: PA287306

Gene: MSH6 HGNC NCBI

ClinVar Allele:

133038

ClinVar RCV:

RCV000216009

RCV000691203

RCV000759861

RCV003997246

ClinVar Variation:

127581

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ala1064Val	CA011826 NM_000179.3:c.3191C>T