Canonical Allele Identifier: PA915975563
Gene: DEFA6 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001917.1:p.Glu35Asp
CA4613010
NM_001926.4:c.105G>C
CA370231753
NM_001926.4:c.105G>T