Canonical Allele Identifier: PA160883
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 134846
ClinVar RCV Id: RCV000121566 RCV000230947 RCV000409685 RCV000571485 RCV000587188 RCV002477316 RCV003483487 RCV003997350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn74His
CA020232
NM_000251.3:c.220A>C