Canonical Allele Identifier: PA2826463224
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408519
ClinVar RCV Id: RCV000457050 RCV000519119 RCV000775712
ClinVar Variation Id: 2010015
ClinVar RCV Id: RCV002842857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn176Lys
CA16611006
NM_001258281.1:c.528C>G
CA346732169
NM_001258281.1:c.528C>A