Allele Registry

Canonical Allele Identifier: PA645379387

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000459417

RCV000479642

RCV000562409

RCV001357378

ClinVar Variation:

410527

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser346Cys	CA16610875 NM_000179.3:c.1037C>G