Allele Registry

Canonical Allele Identifier: PA2499229297

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001323077

ClinVar Variation:

1023084

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gln731Glu	CA346751278 NM_000179.3:c.2191C>G