Canonical Allele Identifier: PA2580133461
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 1959761
ClinVar RCV Id: RCV002701449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025054.1:p.Phe1084Leu
CA346475499
NM_001029883.3:c.3252C>G
CA346475500
NM_001029883.3:c.3252C>A
CA346475506
NM_001029883.3:c.3250T>C