Canonical Allele Identifier: PA2826465737
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773621
ClinVar RCV Id: RCV003584477
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu787Asp
CA346730910
NM_001258281.1:c.2361G>C
CA346730912
NM_001258281.1:c.2361G>T