Canonical Allele Identifier: PA645461507
Gene: ECEL1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004817.2:p.Arg395Gln
CA10581434
NM_004826.4:c.1184G>A