Allele Registry

Canonical Allele Identifier: PA2826587699

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000160704

RCV000168081

RCV000212694

RCV000662520

RCV003330517

RCV003998507

ClinVar Variation:

182651

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Leu1054Phe	CA015417 NM_001281494.2:c.3162G>C CA346761749 NM_001281494.2:c.3162G>T