Canonical Allele Identifier: PA915984092
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127643
ClinVar RCV Id: RCV000115527 RCV000226077 RCV000220764 RCV001257467 RCV003387764 RCV003997278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Tyr55Cys
CA021046
NM_001258281.1:c.164A>G