Allele Registry

Canonical Allele Identifier: PA658680117

Gene: MSH6 HGNC NCBI

ClinVar Allele:

472927

ClinVar RCV:

RCV000572033

RCV000629809

RCV001566523

RCV002265801

RCV003316740

RCV003465183

ClinVar Variation:

480918

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr86Ile	CA46688635 NM_000179.3:c.257C>T