Canonical Allele Identifier: PA211669
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91260
ClinVar RCV Id: RCV000148634 RCV000222150 RCV000412467 RCV000480555 RCV000524426 RCV003997184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser323Cys
CA022662
NM_000251.3:c.968C>G