Allele Registry

Canonical Allele Identifier: PA2826631337

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001323077

ClinVar Variation:

1023084

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Gln429Glu	CA346751278 NM_001281493.2:c.1285C>G