Canonical Allele Identifier: PA645476361
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073620
ClinVar RCV Id: RCV004016626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu908Ile
CA346731785
NM_000251.3:c.2722T>A