Canonical Allele Identifier: PA2826463517
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 233405
ClinVar RCV Id: RCV000219588 RCV000461288 RCV003469076 RCV003998553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Phe247Ser
CA041188
NM_001258281.1:c.740T>C