Allele Registry

Canonical Allele Identifier: PA2741896174

Gene: CCL11 HGNC NCBI

ClinVar RCV:

RCV003974708

ClinVar Variation:

3059737

HGVS (amino-acid)	Matching Registered Transcripts
NP_002977.1:p.Ala23Thr	CA8495693 NM_002986.3:c.67G>A