Canonical Allele Identifier: PA2826464790
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 850718
ClinVar RCV Id: RCV001054948
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro550Ala
CA346728413
NM_001258281.1:c.1648C>G