Canonical Allele Identifier: PA1139712926
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 796109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala260del
CA2580070996
NM_003924.4:c.778_779insGGCGGCGGCGGCAGCGGCAGCGGCGGCAGC
CA2670427141
NM_003924.4:c.774_776del