Canonical Allele Identifier: PA2580299355
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1762577
ClinVar RCV Id: RCV002428030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Pro275Ala
CA356737068
NM_003924.4:c.823C>G