Canonical Allele Identifier: PA2826464884
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1756
ClinVar RCV Id: RCV000001826 RCV000030246 RCV000202104 RCV000491611 RCV001204094 RCV003987305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.His573Tyr
CA019553
NM_001258281.1:c.1717C>T