Canonical Allele Identifier: PA2826624842
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1510444
ClinVar RCV Id: RCV002011774 RCV002255714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gln102Glu
CA346739949
NM_001281492.2:c.304C>G