Allele Registry

Canonical Allele Identifier: PA164713

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000129582

RCV000411815

RCV000479516

RCV000780465

RCV000810760

RCV003460896

RCV003997512

ClinVar Variation:

141188

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Met1202Val	CA013509 NM_000179.3:c.3604A>G