Allele Registry

Canonical Allele Identifier: PA2826630324

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000223633

RCV000467079

RCV001093674

RCV001354875

RCV004532793

ClinVar Variation:

232251

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.His199Tyr	CA067771 NM_001281493.2:c.595C>T