Canonical Allele Identifier: PA1139713180
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 941384
ClinVar RCV Id: RCV001211163 RCV002447076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Thr281Pro
CA356737032
NM_003924.4:c.841A>C