Allele Registry

Canonical Allele Identifier: PA287246

Gene: MSH6 HGNC NCBI

ClinVar Allele:

133009

ClinVar RCV:

RCV000115366

RCV000212641

RCV000469621

ClinVar Variation:

127552

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Pro343Leu	CA007823 NM_000179.3:c.1028C>T