Canonical Allele Identifier: PA645471166
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 231884
ClinVar RCV Id: RCV000222303 RCV000708826 RCV000813496 RCV003469045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala53Ser
CA029624
NM_000251.3:c.157G>T