Allele Registry

Canonical Allele Identifier: PA2826463350

Gene: MSH2 HGNC NCBI

ClinVar Allele:

232550

ClinVar RCV:

RCV000214470

RCV000819833

RCV003156236

ClinVar Variation:

232131

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ser205Tyr	CA10577954 NM_001258281.1:c.614C>A