Canonical Allele Identifier: PA2573231259
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1346897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala257Val
CA356737165
NM_003924.4:c.770C>T