Canonical Allele Identifier: PA645490437
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 362560

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003009.2:p.Ala155Pro
CA4664059
NM_003018.4:c.463G>C