Canonical Allele Identifier: PA915966617
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 820076
ClinVar RCV Id: RCV001013158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr60Ala
CA346729005
NM_000251.3:c.178A>G