Canonical Allele Identifier: PA915997749
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 648649
ClinVar RCV Id: RCV002234956 RCV003133636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly270Val
CA356737101
NM_003924.4:c.809G>T