Canonical Allele Identifier: PA2826465966
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246423
ClinVar RCV Id: RCV000236832 RCV000812576 RCV004532986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys843Gln
CA10584226
NM_001258281.1:c.2527A>C