Canonical Allele Identifier: PA645490279
Gene: SFTPC HGNC NCBI

Linked Data

ClinVar Variation Id: 225466
ClinVar RCV Id: RCV000315399 RCV000490496 RCV002372211 RCV002515598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003009.2:p.Val39Leu
CA4663906
NM_003018.4:c.115G>T
CA370536804
NM_003018.4:c.115G>C