Canonical Allele Identifier: PA658672703
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455523
ClinVar RCV Id: RCV000525389 RCV000573132 RCV001139481 RCV004003739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr594Ile
CA346728292
NM_000251.3:c.1781C>T