Canonical Allele Identifier: PA331719
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91268
ClinVar RCV Id: RCV000076773 RCV000480593 RCV000565059 RCV000684814 RCV001818242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr33Ala
CA022696
NM_000251.3:c.97A>G