Canonical Allele Identifier: PA357698
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 220779
ClinVar RCV Id: RCV000206475 RCV001181937 RCV003468962 RCV003230453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser717Asn
CA034373
NM_000251.3:c.2150G>A