Canonical Allele Identifier: PA093535
Gene: SCNN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 8838
ClinVar RCV Id: RCV000009386 RCV002496312
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000327.2:p.Pro267Leu
CA119964
NM_000336.3:c.800C>T