Allele Registry

Canonical Allele Identifier: PA2826629689

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000580956

RCV000800340

RCV004001261

ClinVar Variation:

489956

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Gln47Glu	CA346741496 NM_001281493.2:c.139C>G