Canonical Allele Identifier: PA2580299354
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2051346
ClinVar RCV Id: RCV002927182

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala274Pro
CA356737074
NM_003924.4:c.820G>C