Allele Registry

Canonical Allele Identifier: PA2826463348

Gene: MSH2 HGNC NCBI

ClinVar Allele:

221217

ClinVar RCV:

RCV000205795

RCV000481152

RCV000657148

RCV001180058

RCV003997604

ClinVar Variation:

220025

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ser205Cys	CA349912 NM_001258281.1:c.614C>G