Canonical Allele Identifier: PA2826462777
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408535
ClinVar RCV Id: RCV000575381 RCV000460763 RCV000523794 RCV004000791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met17Val
CA16610775
NM_001258281.1:c.49A>G