Canonical Allele Identifier: PA658672998
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455558
ClinVar RCV Id: RCV000549300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe784Cys
CA346729967
NM_000251.3:c.2351T>G