Canonical Allele Identifier: PA2825335448
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 578384
ClinVar RCV Id: RCV000701373
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Met471Leu
CA371655383
NM_001024688.3:c.1411A>C
CA371655384
NM_001024688.3:c.1411A>T