Allele Registry

Canonical Allele Identifier: PA2829384197

Gene: MSH5 HGNC NCBI

ClinVar RCV:

RCV003979337

ClinVar Variation:

3056743

HGVS (amino-acid)	Matching Registered Transcripts
NP_002432.1:p.Pro786Ser	CA3721603 NM_002441.5:c.2356C>T