Canonical Allele Identifier: PA2826464201
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 186853
ClinVar RCV Id: RCV000166506 RCV000629905 RCV001355772 RCV003477630 RCV003995508
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys405Asn
CA018242
NM_001258281.1:c.1215A>C
CA346726778
NM_001258281.1:c.1215A>T