Canonical Allele Identifier: PA658663156
Gene: AP2S1 HGNC NCBI

Linked Data

ClinVar Variation Id: 450031
ClinVar RCV Id: RCV000523584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004060.2:p.Leu101Pro
CA406507996
NM_004069.6:c.302T>C