Canonical Allele Identifier: PA915984350
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91110
ClinVar RCV Id: RCV000168725 RCV000491255 RCV000767200 RCV001060501 RCV003444198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly98Trp
CA021215
NM_001258281.1:c.292G>T