Allele Registry

Canonical Allele Identifier: PA2826626483

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002413014

ClinVar Variation:

1781327

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gln488_Leu491del	CA2580067715 NM_001281492.2:c.1461_1472del