Canonical Allele Identifier: PA2580299299
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2479399
ClinVar RCV Id: RCV004267651

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Glu157Gln
CA356738691
NM_003924.4:c.469G>C