Canonical Allele Identifier: PA2573173229
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1521418
ClinVar RCV Id: RCV002031274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000739.1:p.Val222Leu
CA342630575
NM_000748.3:c.664G>C
CA342630576
NM_000748.3:c.664G>T