Canonical Allele Identifier: PA2826462833
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 821880
ClinVar RCV Id: RCV001016750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val29Leu
CA346729592
NM_001258281.1:c.85G>C