Allele Registry

Canonical Allele Identifier: PA645379140

Gene: MSH6 HGNC NCBI

ClinVar Allele:

231541

ClinVar RCV:

RCV000220107

RCV000465049

RCV000566281

RCV001798725

RCV002229338

RCV003998626

ClinVar Variation:

234557

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Arg300Trp	CA073553 NM_000179.3:c.898C>T