Canonical Allele Identifier: PA2826629066
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89476
ClinVar RCV Id: RCV000131709 RCV000454725 RCV000662523 RCV000759868 RCV001082428 RCV001357732 RCV003448259 RCV003492403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr1154Met
CA014580
NM_001281492.2:c.3461C>T