Canonical Allele Identifier: PA2826465609
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1791578
ClinVar RCV Id: RCV002450553 RCV003759739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly754Cys
CA46705349
NM_001258281.1:c.2260G>T