Canonical Allele Identifier: PA2826463722
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 188133
ClinVar RCV Id: RCV000168008 RCV000236761 RCV000568153 RCV000662371 RCV001553594 RCV003995602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu291Ala
CA017027
NM_001258281.1:c.872A>C