Canonical Allele Identifier: PA645474793
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 428539
ClinVar RCV Id: RCV000492007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile624Ser
CA346728486
NM_000251.3:c.1871T>G