Allele Registry

Canonical Allele Identifier: PA2826632863

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000074829

RCV000160725

RCV000524164

RCV000586012

RCV000764430

RCV003149721

ClinVar Variation:

89362

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Pro785Arg	CA012273 NM_001281493.2:c.2354C>G