Allele Registry

Canonical Allele Identifier: PA2826636075

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000160680

RCV000491573

RCV000659892

RCV001850271

ClinVar Variation:

182635

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Pro479Thr	CA010074 NM_001281494.2:c.1435C>A