Canonical Allele Identifier: PA2826465085
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 403109
ClinVar RCV Id: RCV000455798 RCV000699064 RCV001014241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile619Val
CA16609716
NM_001258281.1:c.1855A>G