Allele Registry

Canonical Allele Identifier: PA916012380

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000572899

RCV000797361

ClinVar Variation:

479921

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Lys994Gln	CA072260 NM_001281494.2:c.2980A>C