Canonical Allele Identifier: PA645383152
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232917
ClinVar RCV Id: RCV000218455 RCV000467310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu995Lys
CA10578125
NM_000179.3:c.2983G>A