Allele Registry

Canonical Allele Identifier: PA2825091469

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000805269

RCV001188994

ClinVar Variation:

650169

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu1150Ser	CA346759964 NM_000179.3:c.3449T>C