Allele Registry

Canonical Allele Identifier: PA2826630249

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000480474

RCV001267895

RCV001851230

ClinVar Variation:

422316

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Arg180Gly	CA16617652 NM_001281493.2:c.538C>G