Canonical Allele Identifier: PA2826465752
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479815
ClinVar RCV Id: RCV000575878 RCV000823779 RCV000780442 RCV004000855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile791Met
CA346730953
NM_001258281.1:c.2373T>G