Allele Registry

Canonical Allele Identifier: PA658680170

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000565483

RCV000758664

RCV001858309

ClinVar Variation:

483841

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ala159Thr	CA346738592 NM_000179.3:c.475G>A