Canonical Allele Identifier: PA2573231130
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1383560

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly237Ser
CA356737314
NM_003924.4:c.709G>A