Allele Registry

Canonical Allele Identifier: PA2830033889

Gene: MSH5 HGNC NCBI

ClinVar RCV:

RCV000455959

RCV003970266

ClinVar Variation:

403111

HGVS (amino-acid)	Matching Registered Transcripts
NP_079535.4:p.Pro29Ser	CA3720874 NM_025259.6:c.85C>T