Allele Registry

Canonical Allele Identifier: PA915984148

Gene: MSH2 HGNC NCBI

ClinVar Variation Id: 127645

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ser63Phe	CA021109 NM_001258281.1:c.188C>T