Canonical Allele Identifier: PA2826465143
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90883
ClinVar RCV Id: RCV000076385 RCV000571689 RCV003593899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Cys631Phe
CA019999
NM_001258281.1:c.1892G>T