Canonical Allele Identifier: PA2826875591
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2675388
ClinVar RCV Id: RCV003468087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Glu234Asp
CA381555095
NM_001302959.2:c.702G>C
CA381555100
NM_001302959.2:c.702G>T