Allele Registry

Canonical Allele Identifier: PA891846144

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000697376

RCV001756216

RCV003999664

ClinVar Variation:

575217

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu617Phe	CA346749707 NM_000179.3:c.1849C>T