Allele Registry

Canonical Allele Identifier: PA2825088396

Gene: MSH6 HGNC NCBI

ClinVar Variation Id: 1775540

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser525Arg	CA346746803 NM_000179.3:c.1573A>C CA346746821 NM_000179.3:c.1575T>A CA346746822 NM_000179.3:c.1575T>G