Canonical Allele Identifier: PA2826463448
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 232681
ClinVar RCV Id: RCV000214812 RCV000659880 RCV001067169 RCV003997995
ClinVar Variation Id: 1312637
ClinVar RCV Id: RCV001763643 RCV003163879
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Phe230Leu
CA10577958
NM_001258281.1:c.690C>G
CA346732911
NM_001258281.1:c.688T>C
CA346732916
NM_001258281.1:c.690C>A