Canonical Allele Identifier: PA2579919778
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1718430
ClinVar RCV Id: RCV002299817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe657Ile
CA346728822
NM_000251.3:c.1969T>A