Allele Registry

Canonical Allele Identifier: PA645379738

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000460255

RCV000520334

RCV000567415

RCV004000828

ClinVar Variation:

410392

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Asn404Ser	CA067350 NM_000179.3:c.1211A>G