Canonical Allele Identifier: PA2826462831
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1428995
ClinVar RCV Id: RCV001949990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val29Ala
CA346729596
NM_001258281.1:c.86T>C