Canonical Allele Identifier: PA168901
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142614
ClinVar RCV Id: RCV000131926 RCV003453086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe523Ser
CA018632
NM_000251.3:c.1568T>C