Allele Registry

Canonical Allele Identifier: PA123721

Gene: NPY HGNC NCBI

ClinVar RCV:

RCV000015068

RCV002054440

ClinVar Variation:

14024

HGVS (amino-acid)	Matching Registered Transcripts
NP_000896.1:p.Leu7Pro	CA123720 NM_000905.4:c.20T>C