Canonical Allele Identifier: PA915954368
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 654643
ClinVar RCV Id: RCV000810649 RCV001014223 RCV003492176
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala689Ser
CA46702482
NM_000251.3:c.2065G>T