Canonical Allele Identifier: PA331394
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90801
ClinVar RCV Id: RCV000479241 RCV002408597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Tyr619Cys
CA019445
NM_000251.3:c.1856A>G