Canonical Allele Identifier: PA915984243
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 420893
ClinVar RCV Id: RCV000588981 RCV000771216 RCV001051880 RCV004535515 RCV004003339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val81Gly
CA038774
NM_001258281.1:c.242T>G