Canonical Allele Identifier: PA658673123
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479815
ClinVar RCV Id: RCV000575878 RCV000823779 RCV000780442 RCV004000855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile857Met
CA346730953
NM_000251.3:c.2571T>G