Canonical Allele Identifier: PA331424
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90852
ClinVar RCV Id: RCV000076354 RCV001854322 RCV002415559 RCV003452878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly669Asp
CA019774
NM_000251.3:c.2006G>A