Canonical Allele Identifier: PA645471578
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408505
ClinVar RCV Id: RCV000472699 RCV000572837 RCV001764409 RCV004000783 RCV003226296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile145Thr
CA038704
NM_000251.3:c.434T>C