Canonical Allele Identifier: PA2825385013
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_001034662.3:p.Asn104Ser
CA8792257
NM_001039573.3:c.311A>G