Allele Registry

Canonical Allele Identifier: PA2580266694

Gene: SCGB2A1 HGNC NCBI

ClinVar RCV:

RCV004242923

ClinVar Variation:

2412263

HGVS (amino-acid)	Matching Registered Transcripts
NP_002398.1:p.Met59Thr	CA6042623 NM_002407.3:c.176T>C