Allele Registry

Canonical Allele Identifier: PA2826630774

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001923768

ClinVar Variation:

1421426

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Thr303Pro	CA346749403 NM_001281493.2:c.907A>C