Canonical Allele Identifier: PA2580299302
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1744455
ClinVar RCV Id: RCV002342832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala166Thr
CA356738533
NM_003924.4:c.496G>A