Canonical Allele Identifier: PA2826463042
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408556
ClinVar RCV Id: RCV000458204 RCV000566582 RCV000780450 RCV004000796 RCV004022695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys131Gln
CA039407
NM_001258281.1:c.391A>C