Canonical Allele Identifier: PA913198986
Gene: ERMAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1916
ClinVar RCV Id: RCV000001993 RCV000785148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061008.2:p.Gly57Arg
CA115270
NM_018538.4:c.169G>A
CA339949253
NM_018538.4:c.169G>C