Canonical Allele Identifier: PA2580299356
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1762619
ClinVar RCV Id: RCV002412550

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Pro275Leu
CA356737066
NM_003924.4:c.824C>T