Canonical Allele Identifier: PA2573231302
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1376427
ClinVar RCV Id: RCV001885890 RCV004041072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly272Asp
CA356737086
NM_003924.4:c.815G>A