Allele Registry

Canonical Allele Identifier: PA2826629729

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000485837

RCV000582356

RCV000629703

RCV003464014

RCV004003341

ClinVar Variation:

421018

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Asp55Asn	CA067106 NM_001281493.2:c.163G>A