Canonical Allele Identifier: PA2825187459
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 1482086
ClinVar RCV Id: RCV001994414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000523.2:p.Glu171Asp
CA354739920
NM_000532.5:c.513G>C
CA354739921
NM_000532.5:c.513G>T