Allele Registry

Canonical Allele Identifier: PA2742020092

Gene: MSH5 HGNC NCBI

ClinVar RCV:

RCV003979337

ClinVar Variation:

3056743

HGVS (amino-acid)	Matching Registered Transcripts
NP_751897.1:p.Pro787Ser	CA3721603 NM_172165.4:c.2359C>T