Canonical Allele Identifier: PA2573230892
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1397050
ClinVar RCV Id: RCV001903307
ClinVar Variation Id: 1484316

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala164_Ala167dup
CA2497074312
NM_003924.4:c.486_497dup
CA2573137672
NM_003924.4:c.483_494dup