Canonical Allele Identifier: PA645472133
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 232592
ClinVar RCV Id: RCV000221912 RCV002519711
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn263His
CA10577950
NM_000251.3:c.787A>C