Canonical Allele Identifier: PA2826465417
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 421405
ClinVar RCV Id: RCV000484269 RCV000527665 RCV000563540 RCV003464020 RCV004003352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile700Met
CA16617601
NM_001258281.1:c.2100A>G