Canonical Allele Identifier: PA2826464821
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 427606
ClinVar RCV Id: RCV002413352 RCV000780453 RCV003449268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro556Gln
CA346728465
NM_001258281.1:c.1667C>A