Canonical Allele Identifier: PA2573230996
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1364611
ClinVar RCV Id: RCV001905485 RCV002359308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Pro206Ser
CA2901474
NM_003924.4:c.616C>T