Canonical Allele Identifier: PA645474357
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 420083
ClinVar RCV Id: RCV000485109 RCV000698504 RCV000572164 RCV003470555 RCV004003319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu478Phe
CA16617579
NM_000251.3:c.1432C>T