Canonical Allele Identifier: PA299353
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182577
ClinVar RCV Id: RCV000492034 RCV000587688 RCV000629990 RCV000986650 RCV003998482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser129Cys
CA021106
NM_000251.3:c.386C>G