Allele Registry

Canonical Allele Identifier: PA2826634321

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000566160

RCV001055886

RCV003332204

RCV004001058

ClinVar Variation:

483814

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ser28Pro	CA073692 NM_001281494.2:c.82T>C