Canonical Allele Identifier: PA645506545
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 428851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000255.2:p.Thr1133Ala
CA374111755
NM_000264.5:c.3397A>G