Canonical Allele Identifier: PA658664459
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 467750

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly272Ser
CA356737090
NM_003924.4:c.814G>A