Canonical Allele Identifier: PA2826465031
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90861
ClinVar RCV Id: RCV000076363 RCV000254985 RCV002415560 RCV003452882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly608Asp
CA019835
NM_001258281.1:c.1823G>A