Canonical Allele Identifier: PA2741904038
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2778902
ClinVar RCV Id: RCV003633771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly225Arg
CA95828512
NM_003924.4:c.673G>A
CA356737438
NM_003924.4:c.673G>C