Allele Registry

Canonical Allele Identifier: PA2573163371

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001923768

ClinVar Variation:

1421426

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr605Pro	CA346749403 NM_000179.3:c.1813A>C