Canonical Allele Identifier: PA916012290
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455294
ClinVar RCV Id: RCV001178801 RCV000555651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu972Gln
CA346761247
NM_001281494.2:c.2914G>C