Canonical Allele Identifier: PA645471149
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230706
ClinVar RCV Id: RCV000221582 RCV000526475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly40Val
CA10577918
NM_000251.3:c.119G>T