Canonical Allele Identifier: PA2580299352
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1761637
ClinVar RCV Id: RCV002419210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly267Ala
CA356737115
NM_003924.4:c.800G>C