Canonical Allele Identifier: PA915984320
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91104
ClinVar RCV Id: RCV000076607 RCV000490837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val95Asp
CA021196
NM_001258281.1:c.284T>A