Canonical Allele Identifier: PA2826462797
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 231690
ClinVar RCV Id: RCV000216857 RCV000235359 RCV001320134 RCV002254690 RCV003997919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ser21Tyr
CA10577927
NM_001258281.1:c.62C>A