Canonical Allele Identifier: PA2741933547
Gene: SEC63 HGNC NCBI

Linked Data

ClinVar Variation Id: 3012770
ClinVar RCV Id: RCV003877881
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009145.1:p.Ala626Val
CA365329755
NM_007214.5:c.1877C>T