Canonical Allele Identifier: PA658804082
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 525729
ClinVar RCV Id: RCV000777516 RCV000629968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg711Leu
CA346729289
NM_000251.3:c.2132G>T