Canonical Allele Identifier: PA2741904050
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2797241
ClinVar RCV Id: RCV003634451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Pro232Leu
CA356737362
NM_003924.4:c.695C>T