Allele Registry

Canonical Allele Identifier: PA2826629128

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000572899

RCV000797361

ClinVar Variation:

479921

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Lys1166Gln	CA072260 NM_001281492.2:c.3496A>C