Canonical Allele Identifier: PA2580299358
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1998814
ClinVar RCV Id: RCV002796985

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Pro277His
CA356737054
NM_003924.4:c.830C>A