Canonical Allele Identifier: PA2826464665
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142685
ClinVar RCV Id: RCV000132041 RCV000204826 RCV002466445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro525Leu
CA019258
NM_001258281.1:c.1574C>T