Canonical Allele Identifier: PA2826464192
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455490
ClinVar RCV Id: RCV000550095 RCV001755785 RCV000575666 RCV004003733 RCV004527635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu403Val
CA028542
NM_001258281.1:c.1207C>G