Allele Registry

Canonical Allele Identifier: PA916012269

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000570586

RCV000630109

RCV001174877

RCV003126822

ClinVar Variation:

479931

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Met968Lys	CA072169 NM_001281494.2:c.2903T>A