Canonical Allele Identifier: PA915983960
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 822657
ClinVar RCV Id: RCV001018181 RCV001860896
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu35Gly
CA346729631
NM_001258281.1:c.104A>G