Canonical Allele Identifier: PA658807211
Gene: SFTPD HGNC NCBI

Linked Data

ClinVar Variation Id: 504740
ClinVar RCV Id: RCV000615319
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003010.4:p.Ala295Thr
CA5575022
NM_003019.5:c.883G>A