Canonical Allele Identifier: PA658672711
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455524
ClinVar RCV Id: RCV000542666 RCV002404371 RCV003459178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu595Phe
CA346728296
NM_000251.3:c.1783C>T