Canonical Allele Identifier: PA915984242
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408460
ClinVar RCV Id: RCV000568213 RCV000458857 RCV000759835 RCV003449128 RCV004000775
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val81Ile
CA038750
NM_001258281.1:c.241G>A