Allele Registry

Canonical Allele Identifier: PA658802604

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000630235

RCV000777010

ClinVar Variation:

525870

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu1356Val	CA346761745 NM_000179.3:c.4066T>G