Allele Registry

Canonical Allele Identifier: PA645385141

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000466998

RCV000775745

RCV001555679

RCV003470467

RCV004001844

ClinVar Variation:

410491

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu1330Val	CA16610987 NM_000179.3:c.3988C>G