Canonical Allele Identifier: PA312852
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 203897
ClinVar RCV Id: RCV000186103 RCV002513961 RCV003380511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000911.2:p.Lys589Asn
CA312851
NM_000920.4:c.1767G>T
CA381495040
NM_000920.4:c.1767G>C