Allele Registry

Canonical Allele Identifier: PA330550

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000572978

RCV001222841

RCV003450976

ClinVar Variation:

89442

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr1219Ile	CA013759 NM_000179.3:c.3656C>T