Canonical Allele Identifier: PA2826464387
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142614
ClinVar RCV Id: RCV000131926 RCV003453086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Phe457Ser
CA018632
NM_001258281.1:c.1370T>C