Canonical Allele Identifier: PA658738995
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 489930
ClinVar RCV Id: RCV000580145 RCV001764699
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Tyr678Cys
CA346729119
NM_000251.3:c.2033A>G