Canonical Allele Identifier: PA2826018456
Gene: PALLD HGNC NCBI

Linked Data

ClinVar Variation Id: 348026
ClinVar RCV Id: RCV000389359 RCV004021944
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159580.1:p.Lys22Arg
CA3135287
NM_001166108.2:c.65A>G