Canonical Allele Identifier: PA2829605409
Gene: SFTPA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 227942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005402.3:p.Val19Ala
CA5574371
NM_005411.5:c.56T>C