Allele Registry

Canonical Allele Identifier: PA2825088163

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002381145

ClinVar Variation:

1771267

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Phe461del	CA2580067579 NM_000179.3:c.1380_1382del