Allele Registry

Canonical Allele Identifier: PA645385106

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000480936

RCV000574295

RCV001348367

RCV004002305

ClinVar Variation:

419537

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Met1326Thr	CA072409 NM_000179.3:c.3977T>C