Allele Registry

Canonical Allele Identifier: PA2826636008

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_001268423.1:p.Thr465Ser	CA068780 NM_001281494.2:c.1393A>T CA068793 NM_001281494.2:c.1394C>G