Allele Registry

Canonical Allele Identifier: PA2826630167

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002381145

ClinVar Variation:

1771267

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Phe159del	CA2580067579 NM_001281493.2:c.474_476del