Canonical Allele Identifier: PA915984370
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91111
ClinVar RCV Id: RCV000076614 RCV000630010 RCV003584547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Tyr99Asp
CA021222
NM_001258281.1:c.295T>G