Allele Registry

Canonical Allele Identifier: PA2826628417

Gene: MSH6 HGNC NCBI

ClinVar Allele:

630336

ClinVar RCV:

RCV000805269

RCV001188994

ClinVar Variation:

650169

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Leu1020Ser	CA346759964 NM_001281492.2:c.3059T>C