Canonical Allele Identifier: PA190949
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90999
ClinVar RCV Id: RCV000164439 RCV000484878 RCV000541354 RCV000656884 RCV000663223 RCV001356683 RCV003997165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu853Ala
CA020731
NM_000251.3:c.2558A>C