Canonical Allele Identifier: PA645475511
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246264
ClinVar RCV Id: RCV000236064 RCV000556812 RCV000564620 RCV003469187 RCV003998917
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp742Asn
CA10584222
NM_000251.3:c.2224G>A