Canonical Allele Identifier: PA2826465466
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1789819
ClinVar RCV Id: RCV002448259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Phe714Ser
CA346729938
NM_001258281.1:c.2141T>C