Canonical Allele Identifier: PA916011378
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186361
ClinVar RCV Id: RCV000165943 RCV000198283 RCV000202247 RCV000588416 RCV000758680 RCV003462194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg946His
CA012072
NM_001281492.2:c.2837G>A