Canonical Allele Identifier: PA658681400
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455278
ClinVar RCV Id: RCV000550158 RCV002350168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu1234Lys
CA46719352
NM_000179.3:c.3700_3702delinsAAG
CA346760977
NM_000179.3:c.3700G>A