Canonical Allele Identifier: PA2826463901
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455475
ClinVar RCV Id: RCV000550490 RCV001141978 RCV002225648 RCV002341256 RCV004003727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala332Thr
CA46702776
NM_001258281.1:c.994G>A