Canonical Allele Identifier: PA2580299353
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1761837
ClinVar RCV Id: RCV002419349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Pro269Ser
CA356737108
NM_003924.4:c.805C>T