Canonical Allele Identifier: PA2741904102
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2621280

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala248Thr
CA356737219
NM_003924.4:c.742G>A