Canonical Allele Identifier: PA2580299345
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2445252
ClinVar RCV Id: RCV003154662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala259Gly
CA356737155
NM_003924.4:c.776C>G