Canonical Allele Identifier: PA2829456463
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 3223600
ClinVar RCV Id: RCV004511415
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gln271Cys
CA2825001293
NM_003924.4:c.810_813delinsCTGC