Allele Registry

Canonical Allele Identifier: PA2826632519

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000565431

RCV000573950

RCV001221506

RCV001233423

RCV001551755

RCV002465720

RCV004000885

RCV004001060

ClinVar Variation:

479950

483827

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Thr708Ser	CA346756455 NM_001281493.2:c.2122A>T CA346756458 NM_001281493.2:c.2123C>G