Canonical Allele Identifier: PA2826789009
Gene: ECEL1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001277716.1:p.Cys758Arg
CA150590
NM_001290787.1:c.2272T>C