Canonical Allele Identifier: PA2826465700
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1792751
ClinVar RCV Id: RCV002433198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys779Asn
CA346730807
NM_001258281.1:c.2337A>C
CA346730809
NM_001258281.1:c.2337A>T