Allele Registry

Canonical Allele Identifier: PA2826629935

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000460255

RCV000520334

RCV000567415

RCV004000828

ClinVar Variation:

410392

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Asn102Ser	CA067350 NM_001281493.2:c.305A>G