Canonical Allele Identifier: PA115271
Gene: ERMAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017922.1:p.Gly57Arg
CA115270
NM_001017922.2:c.169G>A
CA339949253
NM_001017922.2:c.169G>C