Canonical Allele Identifier: PA150441
Gene: CHRNA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 98330
ClinVar RCV Id: RCV000084620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000735.1:p.Ser206Thr
CA150440
NM_000744.7:c.617G>C