Canonical Allele Identifier: PA916042898
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 216366
ClinVar Variation Id: 2028643
ClinVar RCV Id: RCV002863572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341847.1:p.Phe376Leu
CA337678
NM_001354918.1:c.1128C>G
CA374119404
NM_001354918.1:c.1128C>A
CA374119409
NM_001354918.1:c.1126T>C