Canonical Allele Identifier: PA915997690
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 826872
ClinVar RCV Id: RCV001026099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly239Cys
CA356737289
NM_003924.4:c.715G>T