Allele Registry

Canonical Allele Identifier: PA2826637344

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000168205

RCV000567226

RCV000656897

RCV000662609

RCV002324752

RCV003997247

ClinVar Variation:

127582

1729213

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Val776Leu	CA012092 NM_001281494.2:c.2326G>C CA346758051 NM_001281494.2:c.2326G>T