Canonical Allele Identifier: PA2826064014
Gene: EFHC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 205391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165891.1:p.Val254Leu
CA314418
NM_001172420.2:c.760G>T
CA364452754
NM_001172420.2:c.760G>C