Canonical Allele Identifier: PA2741887069
Gene: ARVCF HGNC NCBI

Linked Data

ClinVar Variation Id: 2593635
ClinVar RCV Id: RCV004337631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001661.1:p.Ser887Arg
CA10104961
NM_001670.3:c.2661C>G
CA410693398
NM_001670.3:c.2661C>A
CA410693403
NM_001670.3:c.2659A>C