Canonical Allele Identifier: PA2826463309
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408483
ClinVar RCV Id: RCV000473312 RCV000587461 RCV001026892
ClinVar Variation Id: 921168
ClinVar RCV Id: RCV001180427 RCV001316892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu196Asp
CA040426
NM_001258281.1:c.588G>C
CA16611010
NM_001258281.1:c.588G>T