Canonical Allele Identifier: PA2825044773
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 365088
ClinVar RCV Id: RCV000315391 RCV000757218 RCV001201388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Lys439Thr
CA5252800
NM_000118.3:c.1316A>C