Canonical Allele Identifier: PA2826465694
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_001245210.1:p.Cys777Ser
CA346730774
NM_001258281.1:c.2329T>A
CA346730781
NM_001258281.1:c.2330G>C