Allele Registry

Canonical Allele Identifier: PA357566

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000205461

RCV000483247

RCV000567183

RCV000662497

RCV001193121

ClinVar Variation:

219881

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Arg121Cys	CA071503 NM_000179.3:c.361C>T