Canonical Allele Identifier: PA2579909264
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1767524
ClinVar RCV Id: RCV002385287 RCV003094840 RCV003464502
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr32Ile
CA346728743
NM_000251.3:c.95C>T