Canonical Allele Identifier: PA645474696
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408506
ClinVar RCV Id: RCV000467112 RCV001013110 RCV004000784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln593Glu
CA16611035
NM_000251.3:c.1777C>G