Canonical Allele Identifier: PA161480
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 135034
ClinVar RCV Id: RCV000121807 RCV000757604 RCV002354308 RCV001210723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Pro206Arg
CA161478
NM_003924.4:c.617C>G