Canonical Allele Identifier: PA2826465596
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 229933
ClinVar RCV Id: RCV000221679 RCV000985803 RCV001236583 RCV003153497 RCV003997783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln750Arg
CA035821
NM_001258281.1:c.2249A>G