Canonical Allele Identifier: PA2826465631
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1171566
ClinVar RCV Id: RCV001524763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Phe760Leu
CA346730583
NM_001258281.1:c.2278T>C
CA346730593
NM_001258281.1:c.2280T>A
CA346730595
NM_001258281.1:c.2280T>G