Canonical Allele Identifier: PA2826465214
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90907
ClinVar RCV Id: RCV000574384 RCV000535935 RCV004537294 RCV003997159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala648Val
CA020132
NM_001258281.1:c.1943C>T