Allele Registry

Canonical Allele Identifier: PA658664384

Gene: PHOX2B HGNC NCBI

ClinVar Variation Id: 467731

HGVS (amino-acid)	Matching Registered Transcripts
NP_003915.2:p.Ala19Gly	CA356741227 NM_003924.4:c.56C>G