Canonical Allele Identifier: PA915984018
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479788
ClinVar RCV Id: RCV000572927 RCV001575414 RCV001858103 RCV003320690 RCV003459289 RCV004000847
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly42Val
CA346729713
NM_001258281.1:c.125G>T