Canonical Allele Identifier: PA2580299359
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2448119
ClinVar RCV Id: RCV003168185

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Thr281Ile
CA356737023
NM_003924.4:c.842C>T