Allele Registry

Canonical Allele Identifier: PA916011912

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000805269

RCV001188994

ClinVar Variation:

650169

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Leu848Ser	CA346759964 NM_001281494.2:c.2543T>C