Canonical Allele Identifier: PA916002420
Gene: EPB41L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 402208
ClinVar RCV Id: RCV000454281
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036288.2:p.Arg638Cys
CA16609541
NM_012156.2:c.1912C>T