Canonical Allele Identifier: PA2580299325
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1754391
ClinVar RCV Id: RCV002375819
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Pro220Gln
CA356737474
NM_003924.4:c.659C>A