Allele Registry

Canonical Allele Identifier: PA645381867

Gene: MSH6 HGNC NCBI

ClinVar Allele:

405897

ClinVar RCV:

RCV000542142

RCV000580933

RCV000662407

RCV000765686

RCV001284514

RCV004002290

ClinVar Variation:

419197

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr767Ser	CA068780 NM_000179.3:c.2299A>T CA068793 NM_000179.3:c.2300C>G