Allele Registry

Canonical Allele Identifier: PA916011592

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000481708

RCV000564150

RCV000697119

ClinVar Variation:

418643

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ala40Val	CA067043 NM_001281494.2:c.119C>T