Allele Registry

Canonical Allele Identifier: PA2826636666

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000480774

RCV000774604

RCV001071302

RCV003387852

RCV003470525

RCV004002247

ClinVar Variation:

418328

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.His616Arg	CA069591 NM_001281494.2:c.1847A>G