Canonical Allele Identifier: PA915953978
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 651698
ClinVar RCV Id: RCV000807109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala600Thr
CA031405
NM_000251.3:c.1798G>A