Allele Registry

Canonical Allele Identifier: PA339281

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000200387

RCV000482736

RCV001021786

RCV003997001

ClinVar Variation:

216317

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr1355Ser	CA339279 NM_000179.3:c.4064C>G CA346761741 NM_000179.3:c.4063A>T