Allele Registry

Canonical Allele Identifier: PA2826624927

Gene: MSH6 HGNC NCBI

ClinVar Allele:

95038

ClinVar RCV:

RCV000215096

RCV000220612

RCV000630227

RCV000662409

RCV003460703

RCV003997102

ClinVar Variation:

89564

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ile121Val	CA016421 NM_001281492.2:c.361A>G