Canonical Allele Identifier: PA206567
Gene: PHC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 211897
ClinVar RCV Id: RCV000193228 RCV000763869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004417.2:p.Arg876Trp
CA206566
NM_004426.3:c.2626C>T