Canonical Allele Identifier: PA2579909227
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1765043
ClinVar RCV Id: RCV002376052 RCV003759650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro30Ser
CA346728721
NM_000251.3:c.88C>T