Canonical Allele Identifier: PA913192956
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 619867
ClinVar RCV Id: RCV000759830

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys110Asn
CA346730000
NM_000251.3:c.330G>T
CA346730003
NM_000251.3:c.330G>C