Canonical Allele Identifier: PA2826970444
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 2500719
ClinVar RCV Id: RCV003225631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304707.1:p.Pro148Leu
CA4664058
NM_001317778.2:c.443C>T