Canonical Allele Identifier: PA915997620
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 639964
ClinVar RCV Id: RCV002233841
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ser178Thr
CA356738302
NM_003924.4:c.532T>A