Canonical Allele Identifier: PA161477
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 135033
ClinVar RCV Id: RCV000121806 RCV001344362 RCV002354307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly20Ala
CA161475
NM_003924.4:c.59G>C