Canonical Allele Identifier: PA331351
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90745
ClinVar RCV Id: RCV000410128 RCV000484663 RCV000524354 RCV000568086 RCV001198848 RCV003997152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu561Lys
CA018988
NM_000251.3:c.1681G>A