Canonical Allele Identifier: PA2826464868
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1349456
ClinVar RCV Id: RCV002046951
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys569Asn
CA346728612
NM_001258281.1:c.1707A>C
CA346728613
NM_001258281.1:c.1707A>T