Allele Registry

Canonical Allele Identifier: PA658680852

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000570519

RCV000802427

RCV004000872

ClinVar Variation:

479899

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr720Ile	CA068511 NM_000179.3:c.2159C>T