Allele Registry

Canonical Allele Identifier: PA169068

Gene: MSH6 HGNC NCBI

ClinVar Allele:

152377

ClinVar RCV:

RCV000132010

RCV000234247

RCV000412120

RCV000484116

RCV000708888

ClinVar Variation:

142663

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ala1151Gly	CA012948 NM_000179.3:c.3452C>G