Canonical Allele Identifier: PA2826464315
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127630
ClinVar RCV Id: RCV000115502 RCV000222010 RCV001527007 RCV000475133 RCV003460819 RCV004529930 RCV003997270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asp436Gly
CA018475
NM_001258281.1:c.1307A>G