Canonical Allele Identifier: PA645417821
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 404265
ClinVar Variation Id: 998999
ClinVar RCV Id: RCV001294937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004055.1:p.Pro95Ser
CA6457447
NM_004064.5:c.283C>T
CA2017047685
NM_004064.5:c.282_283delinsTT