Canonical Allele Identifier: PA2573230906
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1404632

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Asn169Lys
CA356738449
NM_003924.4:c.507C>G
CA356738452
NM_003924.4:c.507C>A