Canonical Allele Identifier: PA645504980
Gene: SFTPA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 227942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001087239.2:p.Val34Ala
CA5574371
NM_001093770.3:c.101T>C