Allele Registry

Canonical Allele Identifier: PA2830348050

Gene: MSH5 HGNC NCBI

ClinVar RCV:

RCV003979337

ClinVar Variation:

3056743

HGVS (amino-acid)	Matching Registered Transcripts
NP_751898.1:p.Pro786Ser	CA3721603 NM_172166.4:c.2356C>T