Canonical Allele Identifier: PA2826463336
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408531
ClinVar RCV Id: RCV001358282 RCV001027097 RCV002230810 RCV003470449
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ser202Leu
CA040677
NM_001258281.1:c.605C>T