Canonical Allele Identifier: PA117904
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 6011
ClinVar RCV Id: RCV000006382 RCV002227997 RCV002433444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Arg100Leu
CA117902
NM_003924.4:c.299G>T