Allele Registry

Canonical Allele Identifier: PA2826625827

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000700974

RCV003165866

ClinVar Variation:

578073

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Pro332Leu	CA346745042 NM_001281492.2:c.995C>T