Canonical Allele Identifier: PA2826463145
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91174
ClinVar RCV Id: RCV000569759 RCV000662390 RCV000684803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile158Met
CA021724
NM_001258281.1:c.474C>G