Canonical Allele Identifier: PA2573232001
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1516459
ClinVar RCV Id: RCV002040846
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Val49Leu
CA224163199
NM_003977.4:c.145G>T
CA381546571
NM_003977.4:c.145G>C