Canonical Allele Identifier: PA915984193
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 419266
ClinVar RCV Id: RCV000759834 RCV000773079 RCV001246708 RCV003470539 RCV004002296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met75Thr
CA038657
NM_001258281.1:c.224T>C