Allele Registry

Canonical Allele Identifier: PA2826626464

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002031433

RCV003161308

RCV003464402

ClinVar Variation:

1524054

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ser482Leu	CA346749582 NM_001281492.2:c.1445C>T