Canonical Allele Identifier: PA2826628812
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455278
ClinVar RCV Id: RCV000550158 RCV002350168
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu1104Lys
CA46719352
NM_001281492.2:c.3310_3312delinsAAG
CA346760977
NM_001281492.2:c.3310G>A