Canonical Allele Identifier: PA658672410
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455490
ClinVar RCV Id: RCV000550095 RCV001755785 RCV000575666 RCV004003733 RCV004527635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu469Val
CA028542
NM_000251.3:c.1405C>G