Canonical Allele Identifier: PA645434405
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 343467
ClinVar RCV Id: RCV000325301 RCV001706552 RCV003950206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000523.2:p.Pro199Ser
CA2631791
NM_000532.5:c.595C>T