Allele Registry

Canonical Allele Identifier: PA338865

Gene: MSH6 HGNC NCBI

ClinVar Allele:

212253

ClinVar RCV:

RCV000199786

RCV000215044

RCV001194335

RCV003491941

RCV003996999

ClinVar Variation:

216310

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Arg1034Gln	CA070049 NM_000179.3:c.3101G>A