Canonical Allele Identifier: PA2826463681
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 422795
ClinVar RCV Id: RCV000480250 RCV001355929 RCV003485590 RCV003766712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro283Thr
CA16617573
NM_001258281.1:c.847C>A