Canonical Allele Identifier: PA2827551381
Gene: SNX14 HGNC NCBI

Linked Data

ClinVar Variation Id: 419155
ClinVar RCV Id: RCV000485240 RCV003225944
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337479.1:p.Asp537Ter
CA16618336
NM_001350550.2:c.1609_1615del