Allele Registry

Canonical Allele Identifier: PA2825091861

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001804702

ClinVar Variation:

1332186

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser1195Asn	CA346760521 NM_000179.3:c.3584G>A