Canonical Allele Identifier: PA2826970459
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 13210
ClinVar RCV Id: RCV000014097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304707.1:p.Leu182Gln
CA210540
NM_001317778.2:c.545T>A