Canonical Allele Identifier: PA2826629874
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428396
ClinVar RCV Id: RCV000491971 RCV001805109 RCV002523981 RCV004003461
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asp88Glu
CA067253
NM_001281493.2:c.264T>A
CA346742313
NM_001281493.2:c.264T>G