Canonical Allele Identifier: PA2826463326
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 491841
ClinVar RCV Id: RCV000582876 RCV001853922 RCV003459445 RCV003493677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val199Phe
CA346732736
NM_001258281.1:c.595G>T