Canonical Allele Identifier: PA2826465492
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790186
ClinVar RCV Id: RCV002457714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr722Ser
CA346730014
NM_001258281.1:c.2164A>T
CA346730020
NM_001258281.1:c.2165C>G