Canonical Allele Identifier: PA2826628380
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89381
ClinVar RCV Id: RCV000115415 RCV000212683 RCV000524175 RCV000656899 RCV001357449 RCV002288562 RCV003460683 RCV003997089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr1012Met
CA012799
NM_001281492.2:c.3035C>T