Canonical Allele Identifier: PA645471167
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 229782
ClinVar RCV Id: RCV000220104 RCV000679293 RCV000814579 RCV003997771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala54Thr
CA10577921
NM_000251.3:c.160G>A