Canonical Allele Identifier: PA2741933547
Gene: SEC63 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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