Canonical Allele Identifier: PA2826462749
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1022240
ClinVar RCV Id: RCV001788459 RCV001322124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln10Pro
CA346729478
NM_001258281.1:c.29A>C