Canonical Allele Identifier: PA2579922833
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1722340
ClinVar RCV Id: RCV002302454 RCV002427774 RCV003098017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.His839Tyr
CA346730733
NM_000251.3:c.2515C>T