Canonical Allele Identifier: PA2826464690
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1332149
ClinVar RCV Id: RCV001804665
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn530Lys
CA46700072
NM_001258281.1:c.1590T>A
CA346728303
NM_001258281.1:c.1590T>G