Allele Registry

Canonical Allele Identifier: PA645384294

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000457877

RCV000490961

RCV002496783

RCV003148746

RCV003463944

RCV004001861

ClinVar Variation:

410535

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.His1203Asn	CA16610976 NM_000179.3:c.3607C>A