Canonical Allele Identifier: PA2826627717
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127573
ClinVar RCV Id: RCV000115394 RCV000535809 RCV000583327 RCV003997242
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asp774Glu
CA010773
NM_001281492.2:c.2322T>G
CA346755341
NM_001281492.2:c.2322T>A