Canonical Allele Identifier: PA658672579
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 485840
ClinVar RCV Id: RCV000570016 RCV003459387 RCV003767224
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val542Ala
CA346727945
NM_000251.3:c.1625T>C