Allele Registry

Canonical Allele Identifier: PA916011801

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000204403

RCV000519465

RCV000574858

RCV002243887

RCV003462366

RCV003997568

ClinVar Variation:

219569

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.His86Asp	CA067228 NM_001281494.2:c.256C>G