Canonical Allele Identifier: PA2825044774
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 528065
ClinVar RCV Id: RCV000633145 RCV001285345 RCV002385994 RCV003480725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Val440Gly
CA374977914
NM_000118.3:c.1319T>G