Canonical Allele Identifier: PA2826063344
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 362560

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165828.1:p.Ala149Pro
CA4664059
NM_001172357.2:c.445G>C