Canonical Allele Identifier: PA2825862463
Gene: SEC14L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2207579
ClinVar RCV Id: RCV004074230
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137471.2:p.Asn104Ser
CA8792257
NM_001143999.2:c.311A>G