Canonical Allele Identifier: PA2826463423
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408480

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Phe223Leu
CA16611016
NM_001258281.1:c.667T>C
CA346732871
NM_001258281.1:c.669T>G
CA346732872
NM_001258281.1:c.669T>A