Canonical Allele Identifier: PA2741929280
Gene: SCGB1D2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2569208
ClinVar RCV Id: RCV004332819
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006542.1:p.Leu46Pro
CA6042736
NM_006551.4:c.137T>C