Allele Registry

Canonical Allele Identifier: PA2826633703

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000570586

RCV000630109

RCV001174877

RCV003126822

ClinVar Variation:

479931

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Met968Lys	CA072169 NM_001281493.2:c.2903T>A