Canonical Allele Identifier: PA2825044617
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 661587
ClinVar RCV Id: RCV000819037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Cys363Ser
CA374980745
NM_000118.3:c.1088G>C
CA374980747
NM_000118.3:c.1087T>A