Canonical Allele Identifier: PA1139679607
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 978117
ClinVar RCV Id: RCV001256058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Met126Ile
CA342629891
NM_000748.3:c.378G>A
CA342629892
NM_000748.3:c.378G>C
CA342629893
NM_000748.3:c.378G>T