Canonical Allele Identifier: PA2826463207
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408546
ClinVar RCV Id: RCV000456715 RCV002291632 RCV001026093 RCV001843521 RCV004000794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln173Glu
CA16610793
NM_001258281.1:c.517C>G