Canonical Allele Identifier: PA160865
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 134840
ClinVar RCV Id: RCV000121557 RCV000168363 RCV000410801 RCV000512708 RCV000561626 RCV003997346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala2Val
CA021548
NM_000251.3:c.5C>T