Canonical Allele Identifier: PA645434538
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 343473
ClinVar RCV Id: RCV000336865 RCV000727577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000523.2:p.Asn385Ser
CA2632027
NM_000532.5:c.1154A>G