Canonical Allele Identifier: PA2579911312
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 825021
ClinVar RCV Id: RCV001022744 RCV001066450 RCV004004631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser153Phe
CA346730512
NM_000251.3:c.458C>T