Canonical Allele Identifier: PA2826464949
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2453504
ClinVar RCV Id: RCV003182959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val589Leu
CA346728804
NM_001258281.1:c.1765G>C
CA346728805
NM_001258281.1:c.1765G>T