Canonical Allele Identifier: PA1139713088
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 860682
ClinVar RCV Id: RCV003380839 RCV001067037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly268Val
CA2901413
NM_003924.4:c.803G>T