Allele Registry

Canonical Allele Identifier: PA658802158

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000630018

ClinVar Variation:

525753

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu617Arg	CA346749734 NM_000179.3:c.1850T>G