Allele Registry

Canonical Allele Identifier: PA2826629615

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000566160

RCV001055886

RCV003332204

RCV004001058

ClinVar Variation:

483814

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Ser28Pro	CA073692 NM_001281493.2:c.82T>C