Canonical Allele Identifier: PA1139681944
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 927266
ClinVar RCV Id: RCV001370451 RCV001190391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu849Arg
CA346730856
NM_000251.3:c.2546T>G