Canonical Allele Identifier: PA2829037381
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 2435887
ClinVar RCV Id: RCV003136637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372587.1:p.Thr152Met
CA370538265
NM_001385658.1:c.455C>T