Canonical Allele Identifier: PA645474699
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 421094
ClinVar RCV Id: RCV000484616 RCV001013177 RCV001205685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn596His
CA16617589
NM_000251.3:c.1786A>C