Allele Registry

Canonical Allele Identifier: PA2825088765

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003090265

ClinVar Variation:

2165988

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Lys603Glu	CA346749367 NM_000179.3:c.1807A>G