Canonical Allele Identifier: PA2579921415
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1788682
ClinVar RCV Id: RCV002443791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser755Phe
CA346729790
NM_000251.3:c.2264C>T