Canonical Allele Identifier: PA2573230906
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1404632
ClinVar RCV Id: RCV001927791 RCV002344005
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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