Canonical Allele Identifier: PA2741904108
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2725607
ClinVar RCV Id: RCV003518497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Leu263Arg
CA356737135
NM_003924.4:c.788T>G