Allele Registry

Canonical Allele Identifier: PA658680393

Gene: MSH6 HGNC NCBI

ClinVar Allele:

473035

ClinVar RCV:

RCV000566795

RCV000586030

RCV000696871

RCV004000879

ClinVar Variation:

479920

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser315Cys	CA073607 NM_000179.3:c.944C>G