Allele Registry

Canonical Allele Identifier: PA2829384129

Gene: MSH5 HGNC NCBI

ClinVar RCV:

RCV003973883

ClinVar Variation:

3056913

HGVS (amino-acid)	Matching Registered Transcripts
NP_002432.1:p.Leu85Phe	CA3720908 NM_002441.5:c.253C>T