Canonical Allele Identifier: PA331662
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91174
ClinVar RCV Id: RCV000569759 RCV000662390 RCV000684803
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile224Met
CA021724
NM_000251.3:c.672C>G