Canonical Allele Identifier: PA2573165165
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1354604
ClinVar RCV Id: RCV001866507 RCV004009192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile774Met
CA346729897
NM_000251.3:c.2322T>G