Canonical Allele Identifier: PA2573230947
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1471337
ClinVar RCV Id: RCV001975613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Asp182Ala
CA356738221
NM_003924.4:c.545A>C