Canonical Allele Identifier: PA2573231326
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1463309
ClinVar RCV Id: RCV001956604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Pro284Thr
CA356736996
NM_003924.4:c.850C>A