Allele Registry

Canonical Allele Identifier: PA2826630778

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002410236

ClinVar Variation:

1780643

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Thr303Ile	CA346749415 NM_001281493.2:c.908C>T