Canonical Allele Identifier: PA2829456302
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 467741

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala250_Ala260del
CA2901433
NM_003924.4:c.735_767del
CA794914227
NM_003924.4:c.741_773del