Allele Registry

Canonical Allele Identifier: PA269929

Gene: CHRNA1 HGNC NCBI

ClinVar RCV:

RCV000122732

ClinVar Variation:

135654

HGVS (amino-acid)	Matching Registered Transcripts
NP_001034612.1:p.Ser271Tyr	CA269927 NM_001039523.3:c.812C>A