Canonical Allele Identifier: PA2826464518
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483664
ClinVar RCV Id: RCV000570315 RCV000802215 RCV001310202 RCV002497211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ser488Asn
CA030195
NM_001258281.1:c.1463G>A