Canonical Allele Identifier: PA915953685
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 642423
ClinVar RCV Id: RCV000795889

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys546Arg
CA346727974
NM_000251.3:c.1637A>G