Canonical Allele Identifier: PA2826462990
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91133
ClinVar RCV Id: RCV000130716 RCV000202264 RCV000411418 RCV000587046 RCV001081828 RCV001798268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn120Ser
CA021391
NM_001258281.1:c.359A>G