Canonical Allele Identifier: PA210541
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 13210
ClinVar RCV Id: RCV000014097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003009.2:p.Leu188Gln
CA210540
NM_003018.4:c.563T>A