Canonical Allele Identifier: PA2826625691
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127559
ClinVar RCV Id: RCV000115373 RCV000218965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly300Arg
CA008438
NM_001281492.2:c.898G>A
CA346744165
NM_001281492.2:c.898G>C