Canonical Allele Identifier: PA2499265209
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1037073
ClinVar RCV Id: RCV001340170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Asp285Ala
CA356736980
NM_003924.4:c.854A>C