Allele Registry

Canonical Allele Identifier: PA2826625828

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000216959

RCV000800743

ClinVar Variation:

230718

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Pro332Thr	CA10578068 NM_001281492.2:c.994C>A