Allele Registry

Canonical Allele Identifier: PA2829384123

Gene: MSH5 HGNC NCBI

ClinVar RCV:

RCV000455959

RCV003970266

ClinVar Variation:

403111

HGVS (amino-acid)	Matching Registered Transcripts
NP_002432.1:p.Pro29Ser	CA3720874 NM_002441.5:c.85C>T