Canonical Allele Identifier: PA2826063460
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 362562

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165881.1:p.Leu181Val
CA4664075
NM_001172410.2:c.541C>G