Allele Registry

Canonical Allele Identifier: PA2826630832

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002413014

ClinVar Variation:

1781327

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Gln316_Leu319del	CA2580067715 NM_001281493.2:c.945_956del