Canonical Allele Identifier: PA1139713069
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 858862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly268Asp
CA2901414
NM_003924.4:c.803G>A