Canonical Allele Identifier: PA2825997703
Gene: SFTPA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 227942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158116.1:p.Val19Ala
CA5574371
NM_001164644.2:c.56T>C