Allele Registry

Canonical Allele Identifier: PA2499229328

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001322251

RCV001806119

ClinVar Variation:

1022358

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu617Ile	CA068196 NM_000179.3:c.1849C>A