Canonical Allele Identifier: PA645471140
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418943
ClinVar RCV Id: RCV000484906 RCV001016981 RCV001037181 RCV004002277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val34Met
CA16617548
NM_000251.3:c.100G>A