Canonical Allele Identifier: PA2580299351
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2448120
ClinVar RCV Id: RCV003168186

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala266Thr
CA356737123
NM_003924.4:c.796G>A