Canonical Allele Identifier: PA2573230911
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1444821
ClinVar RCV Id: RCV001992450 RCV002334953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly170Ser
CA356738444
NM_003924.4:c.508G>A