Canonical Allele Identifier: PA2826628949
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127593
ClinVar RCV Id: RCV000115423 RCV000121588 RCV000656903 RCV000662548 RCV000764435 RCV001079217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg1133His
CA014284
NM_001281492.2:c.3398G>A