Allele Registry

Canonical Allele Identifier: PA2825088590

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002398956

ClinVar Variation:

1778619

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gln572Arg	CA346748606 NM_000179.3:c.1715A>G