Canonical Allele Identifier: PA192495
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90682
ClinVar RCV Id: RCV000076178 RCV000165088 RCV000412350 RCV000486935 RCV000524345 RCV000781557 RCV001030703 RCV001354505 RCV003153355 RCV002513806
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro5Gln
CA018457
NM_000251.3:c.14C>A