Allele Registry

Canonical Allele Identifier: PA164401

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000129429

RCV000630083

RCV004532551

ClinVar Variation:

141078

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser702Leu	CA009694 NM_000179.3:c.2105C>T