Canonical Allele Identifier: PA2826063899
Gene: EFHC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 205398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165891.1:p.Arg32Trp
CA314432
NM_001172420.2:c.94C>T