Canonical Allele Identifier: PA645434488
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 343470

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000523.2:p.Pro279Leu
CA2631888
NM_000532.5:c.836C>T