Allele Registry

Canonical Allele Identifier: PA2825091855

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001993900

ClinVar Variation:

1469431

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu1193Asp	CA346760509 NM_000179.3:c.3579A>C CA346760510 NM_000179.3:c.3579A>T