Canonical Allele Identifier: PA2826635501
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410524
ClinVar RCV Id: RCV000458338 RCV000562905 RCV004001856 RCV002281095
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp347Gly
CA16610993
NM_001281494.2:c.1040A>G