Canonical Allele Identifier: PA160869
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127632
ClinVar RCV Id: RCV000121559 RCV000122981 RCV000492001 RCV000656878 RCV000662395 RCV003997272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg534His
CA018712
NM_000251.3:c.1601G>A