Allele Registry

Canonical Allele Identifier: PA2830033934

Gene: MSH5 HGNC NCBI

ClinVar RCV:

RCV003979337

ClinVar Variation:

3056743

HGVS (amino-acid)	Matching Registered Transcripts
NP_079535.4:p.Pro774Ser	CA3721603 NM_025259.6:c.2320C>T