Canonical Allele Identifier: PA2826464681
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455523
ClinVar RCV Id: RCV000525389 RCV000573132 RCV001139481 RCV004003739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr528Ile
CA346728292
NM_001258281.1:c.1583C>T