Allele Registry

Canonical Allele Identifier: PA2825088840

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV004520667

ClinVar Variation:

3230516

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gln618Arg	CA068201 NM_000179.3:c.1853A>G