Canonical Allele Identifier: PA2573177607
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 1350428
ClinVar RCV Id: RCV002051325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025054.1:p.His395Gln
CA1592478
NM_001029883.3:c.1185C>A
CA346480725
NM_001029883.3:c.1185C>G