Canonical Allele Identifier: PA211664
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90660
ClinVar RCV Id: RCV000148630 RCV000218562 RCV000482094 RCV000627720 RCV003997147 RCV003466964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser473Leu
CA018254
NM_000251.3:c.1418C>T