Canonical Allele Identifier: PA1139676044
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 926425
ClinVar RCV Id: RCV001189020 RCV001321132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu7Lys
CA46666445
NM_000251.3:c.19G>A