Allele Registry

Canonical Allele Identifier: PA645505394

Gene: MSH5 HGNC NCBI

ClinVar RCV:

RCV000455959

RCV003970266

ClinVar Variation:

403111

HGVS (amino-acid)	Matching Registered Transcripts
NP_751897.1:p.Pro29Ser	CA3720874 NM_172165.4:c.85C>T