Canonical Allele Identifier: PA2580299360
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2132443
ClinVar RCV Id: RCV003036739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ile283Leu
CA356737010
NM_003924.4:c.847A>C