Canonical Allele Identifier: PA915997752
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 665555
ClinVar RCV Id: RCV002415946 RCV002235461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly272Val
CA356737085
NM_003924.4:c.815G>T