Allele Registry

Canonical Allele Identifier: PA2826630632

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002398931

ClinVar Variation:

1778592

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Gly269Ala	CA346748588 NM_001281493.2:c.806G>C