Canonical Allele Identifier: PA2826464899
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 161299
ClinVar RCV Id: RCV000148637 RCV000160596 RCV000204646 RCV000589876 RCV000765671 RCV003483522 RCV003998170 RCV004532666 RCV002509245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu577Lys
CA019583
NM_001258281.1:c.1729G>A