Canonical Allele Identifier: PA331398
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90805
ClinVar RCV Id: RCV000255200 RCV000491749 RCV001036384 RCV003452863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro622Thr
CA019468
NM_000251.3:c.1864C>A