Allele Registry

Canonical Allele Identifier: PA2826630788

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000196510

RCV000491442

RCV000589796

RCV000757926

RCV002271428

ClinVar Variation:

182626

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Ile306Val	CA009270 NM_001281493.2:c.916A>G