Canonical Allele Identifier: PA658735703
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 489932
ClinVar RCV Id: RCV000580313 RCV000698385 RCV003478306 RCV004001258 RCV004530629
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu7Ala
CA46666467
NM_000251.3:c.20A>C