Canonical Allele Identifier: PA2826464427
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408539
ClinVar RCV Id: RCV000791418 RCV000572859 RCV000986674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val466Ala
CA029661
NM_001258281.1:c.1397T>C