Canonical Allele Identifier: PA279198
Gene: ARMCX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 208887
ClinVar RCV Id: RCV000201323
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243084.2:p.Thr192Ser
CA279197
NM_001256155.3:c.574A>T
CA10473552
NM_001256155.3:c.575C>G