Allele Registry

Canonical Allele Identifier: PA2825088771

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV004015602

ClinVar Variation:

3075076

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu604Ala	CA346749388 NM_000179.3:c.1811A>C