Canonical Allele Identifier: PA1139713172
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 939675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Pro277Leu
CA356737053
NM_003924.4:c.830C>T