Canonical Allele Identifier: PA2829337049
Gene: ARVCF HGNC NCBI

Linked Data

ClinVar Variation Id: 3130000
ClinVar RCV Id: RCV004418345
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001661.1:p.Gly886Val
CA10104964
NM_001670.3:c.2657G>T