Canonical Allele Identifier: PA645471498
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 336426
ClinVar RCV Id: RCV000389495 RCV002323544 RCV003758755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser112Cys
CA037917
NM_000251.3:c.335C>G