Canonical Allele Identifier: PA2826463359
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479806
ClinVar RCV Id: RCV000567448 RCV001071692
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile208Met
CA46683968
NM_001258281.1:c.624C>G