Canonical Allele Identifier: PA645427232
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 239596
ClinVar RCV Id: RCV000229358 RCV001017576 RCV001391323 RCV001145118 RCV003919957 RCV001753699
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly278Ser
CA2901407
NM_003924.4:c.832G>A