Canonical Allele Identifier: PA2830338019
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_722523.1:p.Asp922Ter
CA16618336
NM_153816.6:c.2764_2770del