Canonical Allele Identifier: PA2825044840
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1404798
ClinVar RCV Id: RCV001903408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Phe486Leu
CA374975997
NM_000118.3:c.1458C>G
CA374975998
NM_000118.3:c.1458C>A
CA374976014
NM_000118.3:c.1456T>C