Canonical Allele Identifier: PA2826463188
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3076127
ClinVar RCV Id: RCV004018444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asp170Tyr
CA346732029
NM_001258281.1:c.508G>T