Allele Registry

Canonical Allele Identifier: PA2826633766

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000216678

RCV000704640

RCV000708893

RCV001358640

RCV003469028

ClinVar Variation:

231365

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Glu979Gln	CA10578163 NM_001281493.2:c.2935G>C