Allele Registry

Canonical Allele Identifier: PA2499229369

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001354749

RCV003771036

RCV004036718

ClinVar Variation:

1049095

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser156Leu	CA346738576 NM_000179.3:c.467C>T