Allele Registry

Canonical Allele Identifier: PA2825088161

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003595095

ClinVar Variation:

2710367

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Phe461Tyr	CA346745001 NM_000179.3:c.1382T>A