Canonical Allele Identifier: PA2827550546
Gene: SNX14 HGNC NCBI

Linked Data

ClinVar Variation Id: 419155
ClinVar RCV Id: RCV000485240 RCV003225944
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337470.1:p.Asp858Ter
CA16618336
NM_001350541.2:c.2572_2578del