Allele Registry

Canonical Allele Identifier: PA916011057

Gene: MSH6 HGNC NCBI

ClinVar Allele:

392825

ClinVar RCV:

RCV000459237

RCV000572922

RCV000761153

RCV003335336

RCV003463930

ClinVar Variation:

410430

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ser63Cys	CA16610836 NM_001281492.2:c.188C>G