Canonical Allele Identifier: PA915988619
Gene: SFTPA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 227942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158117.1:p.Val34Ala
CA5574371
NM_001164645.2:c.101T>C