Canonical Allele Identifier: PA2573231312
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1059064
ClinVar RCV Id: RCV001368276
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Pro279_Ile280insSerPro
CA2499217209
NM_003924.4:c.833_838dup