Allele Registry

Canonical Allele Identifier: PA2826634619

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000213558

RCV000568557

RCV000627712

RCV003997065

ClinVar Variation:

89187

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ile140Thr	CA008493 NM_001281494.2:c.419T>C