Canonical Allele Identifier: PA658672688
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479851
ClinVar RCV Id: RCV000562329 RCV000696814 RCV004000863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu590Asp
CA031214
NM_000251.3:c.1770A>C
CA346728270
NM_000251.3:c.1770A>T