Canonical Allele Identifier: PA2826462959
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479811
ClinVar RCV Id: RCV000563802
ClinVar Variation Id: 1361236
ClinVar RCV Id: RCV001865141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Phe112Leu
CA346730799
NM_001258281.1:c.334T>C
CA346730810
NM_001258281.1:c.336C>A
CA346730812
NM_001258281.1:c.336C>G