Canonical Allele Identifier: PA191140
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 185140
ClinVar RCV Id: RCV000164508 RCV000233615 RCV000411131 RCV001762369 RCV003114313
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro30Leu
CA022507
NM_000251.3:c.89C>T