Allele Registry

Canonical Allele Identifier: PA2826633048

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000009496

ClinVar Variation:

89379

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Cys827_Val828delinsLeu	CA012733 NM_001281493.2:c.2480_2482del