Canonical Allele Identifier: PA2829337047
Gene: ARVCF HGNC NCBI

Linked Data

ClinVar Variation Id: 3129998
ClinVar RCV Id: RCV004418343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001661.1:p.Thr838Ser
CA10105079
NM_001670.3:c.2513C>G
CA410694660
NM_001670.3:c.2512A>T