Canonical Allele Identifier: PA915984275
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483732
ClinVar RCV Id: RCV000566316 RCV000764422 RCV000808811 RCV001551071 RCV003459360 RCV004001041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val89Ala
CA346730530
NM_001258281.1:c.266T>C