Canonical Allele Identifier: PA915997688
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 826833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly237Arg
CA356737316
NM_003924.4:c.709G>C