Canonical Allele Identifier: PA2826465363
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 229770
ClinVar RCV Id: RCV000221755 RCV000464199 RCV000780438 RCV001843496 RCV002485413 RCV003997767 RCV004020644
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr688Ser
CA035112
NM_001258281.1:c.2062A>T
CA346729785
NM_001258281.1:c.2063C>G