Canonical Allele Identifier: PA2825082142
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2708471
ClinVar RCV Id: RCV003595056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp231del
CA2697548109
NM_000251.3:c.690_692del