Canonical Allele Identifier: PA658673025
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483746
ClinVar RCV Id: RCV000566106 RCV001224509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.His801Leu
CA346730193
NM_000251.3:c.2402A>T