Canonical Allele Identifier: PA645475820
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 428545
ClinVar RCV Id: RCV000490997 RCV003449375
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.His801Pro
CA346730191
NM_000251.3:c.2402A>C