Canonical Allele Identifier: PA658673076
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483718
ClinVar RCV Id: RCV000565473 RCV004001038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Cys843Ser
CA346730774
NM_000251.3:c.2527T>A
CA346730781
NM_000251.3:c.2528G>C