Canonical Allele Identifier: PA645476353
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 232549
ClinVar RCV Id: RCV000216683 RCV002229281 RCV003997983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile906Met
CA10578017
NM_000251.3:c.2718A>G