Canonical Allele Identifier: PA2826463846
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 620607
ClinVar RCV Id: RCV000761062 RCV001219957 RCV002352272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asp320Asn
CA346733690
NM_001258281.1:c.958G>A