Allele Registry

Canonical Allele Identifier: PA645427232

Gene: PHOX2B HGNC NCBI

ClinVar RCV:

RCV000229358

RCV001017576

RCV001145118

RCV001391323

RCV001753699

RCV003919957

ClinVar Variation:

239596

HGVS (amino-acid)	Matching Registered Transcripts
NP_003915.2:p.Gly278Ser	CA2901407 NM_003924.4:c.832G>A