Canonical Allele Identifier: PA645417791
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 404268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004055.1:p.Pro11Ser
CA6457364
NM_004064.5:c.31C>T