Canonical Allele Identifier: PA658664393
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 467719
ClinVar RCV Id: RCV000545357 RCV001011753 RCV003324762 RCV003476287
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Thr49Asn
CA2901603
NM_003924.4:c.146C>A