Canonical Allele Identifier: PA2826465049
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 231326
ClinVar RCV Id: RCV000221435 RCV002228960 RCV003462461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Tyr612His
CA10577996
NM_001258281.1:c.1834T>C