Canonical Allele Identifier: PA2826465107
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1002257
ClinVar RCV Id: RCV001298657
ClinVar Variation Id: 1055457
ClinVar RCV Id: RCV002420799 RCV001364129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln624His
CA346729181
NM_001258281.1:c.1872A>C
CA346729182
NM_001258281.1:c.1872A>T