Canonical Allele Identifier: PA2499265206
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1172785
ClinVar RCV Id: RCV001647348 RCV002424966 RCV003771626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Pro277Thr
CA356737058
NM_003924.4:c.829C>A