Allele Registry

Canonical Allele Identifier: PA658680747

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000535515

RCV000570791

RCV003470702

ClinVar Variation:

455156

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser616Phe	CA346749690 NM_000179.3:c.1847C>T