Canonical Allele Identifier: PA915964013
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 819298
ClinVar RCV Id: RCV001011735 RCV001862780
ClinVar Variation Id: 2087201
ClinVar RCV Id: RCV002999968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met491Ile
CA346745935
NM_000179.3:c.1473G>A
CA346745943
NM_000179.3:c.1473G>T
CA346745946
NM_000179.3:c.1473G>C