Canonical Allele Identifier: PA2741903994
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2867615
ClinVar RCV Id: RCV003633135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Asp182Gly
CA356738219
NM_003924.4:c.545A>G