Canonical Allele Identifier: PA2826464166
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182558
ClinVar RCV Id: RCV000160583 RCV000198641 RCV000492025 RCV000662679 RCV002265636 RCV003998470
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asp395Ala
CA018117
NM_001258281.1:c.1184A>C