Allele Registry

Canonical Allele Identifier: PA645379521

Gene: MSH6 HGNC NCBI

ClinVar Allele:

232705

ClinVar RCV:

RCV000213418

RCV000791357

RCV001559019

RCV003462454

RCV003993896

RCV003993897

ClinVar Variation:

231103

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu376Gly	CA067175 NM_000179.3:c.1127A>G