Canonical Allele Identifier: PA2825045026
Gene: ENG HGNC NCBI
ClinVar RCV:
RCV000633140
ClinVar Variation:
528060
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Ser615Trp
CA5252623
NM_000118.3:c.1844C>G