Canonical Allele Identifier: PA2826875812
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 41164
ClinVar RCV Id: RCV000034063 RCV000563699 RCV000897518 RCV003894847
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Val49Met
CA344063
NM_001302960.2:c.145G>A