Canonical Allele Identifier: PA658671894
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479794
ClinVar RCV Id: RCV000562138 RCV001222036 RCV004000851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser255Arg
CA346732397
NM_000251.3:c.763A>C
CA346732404
NM_000251.3:c.765T>A
CA346732405
NM_000251.3:c.765T>G