Canonical Allele Identifier: PA2579922931
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1792751
ClinVar RCV Id: RCV002433198

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys845Asn
CA346730807
NM_000251.3:c.2535A>C
CA346730809
NM_000251.3:c.2535A>T