Canonical Allele Identifier: PA2573231303
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1413997
ClinVar RCV Id: RCV001928470

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala274Thr
CA356737075
NM_003924.4:c.820G>A