Canonical Allele Identifier: PA2829037054
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 2435887
ClinVar RCV Id: RCV003136637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372582.1:p.Thr158Met
CA370538265
NM_001385653.1:c.473C>T