Allele Registry

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Canonical Allele Identifier: PA658812301

Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 535772

ClinVar RCV Id: RCV002233517

ClinVar Variation Id: 861479

ClinVar RCV Id: RCV001068011

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_003915.2:p.Gly270Arg	CA356737103 NM_003924.4:c.808G>C CA356737104 NM_003924.4:c.808G>A