Canonical Allele Identifier: PA331361
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1977830
ClinVar RCV Id: RCV002750842 RCV003167708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val57Met
CA019054
NM_000251.3:c.169G>A