Canonical Allele Identifier: PA331229
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90553
ClinVar RCV Id: RCV000487066 RCV000568561 RCV000663061 RCV000703497 RCV003149744 RCV003997141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg382His
CA017350
NM_000251.3:c.1145G>A